Canonical Allele Identifier: CA1768019550

Gene: ASAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061201_18061203delinsAAC , CM000670.2:g.18061201_18061203delinsAAC	GRCh38
NC_000008.10:g.17918710_17918712delinsAAC , CM000670.1:g.17918710_17918712delinsAAC	GRCh37
NC_000008.9:g.17962990_17962992delinsAAC	NCBI36
NG_008985.1:g.28796_28798delinsGTT
NG_008985.2:g.28796_28798delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.833+174_833+176delinsGTT	ENSP00000371152.4:n.833+174_833+176delinsGTT
ENST00000518746.2:n.2471+174_2471+176delinsGTT
ENST00000520781.6:c.710+174_710+176delinsGTT	ENSP00000427751.1:n.710+174_710+176delinsGTT
ENST00000521542.2:n.267_269delinsGTT
ENST00000635756.1:c.198+174_198+176delinsGTT
ENST00000635944.1:c.*621+174_*621+176delinsGTT	ENSP00000490195.1:n.*621+174_*621+176delinsGTT
ENST00000635998.1:c.785+174_785+176delinsGTT	ENSP00000490506.1:n.785+174_785+176delinsGTT
ENST00000636009.1:c.642+174_642+176delinsGTT	ENSP00000489988.1:n.642+174_642+176delinsGTT
ENST00000636033.1:c.*621+174_*621+176delinsGTT	ENSP00000489617.1:n.*621+174_*621+176delinsGTT
ENST00000636050.1:c.*628+174_*628+176delinsGTT	ENSP00000490562.1:n.*628+174_*628+176delinsGTT
ENST00000636128.1:c.464+174_464+176delinsGTT	ENSP00000489789.1:n.464+174_464+176delinsGTT
ENST00000636160.1:c.*677+174_*677+176delinsGTT	ENSP00000489651.1:n.*677+174_*677+176delinsGTT
ENST00000636171.1:c.728+174_728+176delinsGTT	ENSP00000489761.1:n.728+174_728+176delinsGTT
ENST00000636455.1:c.833+174_833+176delinsGTT	ENSP00000490502.1:n.833+174_833+176delinsGTT
ENST00000636494.1:c.*565+174_*565+176delinsGTT	ENSP00000490388.1:n.*565+174_*565+176delinsGTT
ENST00000636563.1:n.447+174_447+176delinsGTT
ENST00000636577.1:c.725+174_725+176delinsGTT	ENSP00000490027.1:n.725+174_725+176delinsGTT
ENST00000636691.1:c.590+174_590+176delinsGTT	ENSP00000490725.1:n.590+174_590+176delinsGTT
ENST00000636701.1:c.*436+174_*436+176delinsGTT	ENSP00000489800.1:n.*436+174_*436+176delinsGTT
ENST00000636815.1:c.702+174_702+176delinsGTT
ENST00000636920.1:c.*621+174_*621+176delinsGTT	ENSP00000490437.1:n.*621+174_*621+176delinsGTT
ENST00000636997.1:c.698+174_698+176delinsGTT	ENSP00000490093.1:n.698+174_698+176delinsGTT
ENST00000637013.1:c.*1153+174_*1153+176delinsGTT	ENSP00000490596.1:n.*1153+174_*1153+176delinsGTT
ENST00000637014.1:n.1192+174_1192+176delinsGTT
ENST00000637095.1:c.*565+174_*565+176delinsGTT	ENSP00000490415.1:n.*565+174_*565+176delinsGTT
ENST00000637244.1:c.*1303+174_*1303+176delinsGTT	ENSP00000490188.1:n.*1303+174_*1303+176delinsGTT
ENST00000637343.1:n.2222+174_2222+176delinsGTT
ENST00000637429.1:c.*997+174_*997+176delinsGTT	ENSP00000490522.1:n.*997+174_*997+176delinsGTT
ENST00000637484.1:c.*747+174_*747+176delinsGTT	ENSP00000490837.1:n.*747+174_*747+176delinsGTT
ENST00000637528.1:c.722+174_722+176delinsGTT	ENSP00000490801.1:n.722+174_722+176delinsGTT
ENST00000637609.1:n.3506+174_3506+176delinsGTT
ENST00000637636.1:c.779+174_779+176delinsGTT	ENSP00000490112.1:n.779+174_779+176delinsGTT
ENST00000637790.2:c.785+174_785+176delinsGTT MANE Select	ENSP00000490272.1:n.785+174_785+176delinsGTT
ENST00000637857.1:n.1151+174_1151+176delinsGTT
ENST00000637922.1:c.590+174_590+176delinsGTT	ENSP00000490071.1:n.590+174_590+176delinsGTT
ENST00000637991.1:c.758+174_758+176delinsGTT	ENSP00000489901.1:n.758+174_758+176delinsGTT
ENST00000638028.1:n.1002+174_1002+176delinsGTT
ENST00000638069.1:n.1606+174_1606+176delinsGTT
ENST00000262097.10:c.785+174_785+176delinsGTT	ENSP00000262097.6:n.785+174_785+176delinsGTT
ENST00000314146.10:c.767+174_767+176delinsGTT	ENSP00000326970.10:n.767+174_767+176delinsGTT
ENST00000381733.8:c.833+174_833+176delinsGTT	ENSP00000371152.4:n.833+174_833+176delinsGTT
ENST00000519468.5:n.614+174_614+176delinsGTT
ENST00000520781.5:c.710+174_710+176delinsGTT	ENSP00000427751.1:n.710+174_710+176delinsGTT
ENST00000521542.1:n.498+174_498+176delinsGTT
NM_001127505.1:c.767+174_767+176delinsGTT	NP_001120977.1:n.767+174_767+176delinsGTT
NM_001127505.2:c.767+174_767+176delinsGTT	NP_001120977.1:n.767+174_767+176delinsGTT
NM_004315.4:c.833+174_833+176delinsGTT	NP_004306.3:n.833+174_833+176delinsGTT
NM_004315.5:c.833+174_833+176delinsGTT	NP_004306.3:n.833+174_833+176delinsGTT
NM_177924.3:c.785+174_785+176delinsGTT	NP_808592.2:n.785+174_785+176delinsGTT
NM_177924.4:c.785+174_785+176delinsGTT	NP_808592.2:n.785+174_785+176delinsGTT
XM_005273504.2:c.719+174_719+176delinsGTT	XP_005273561.1:n.719+174_719+176delinsGTT
NM_001363743.1:c.590+174_590+176delinsGTT	NP_001350672.1:n.590+174_590+176delinsGTT
XM_005273504.3:c.719+174_719+176delinsGTT	XP_005273561.1:n.719+174_719+176delinsGTT
NM_177924.5:c.785+174_785+176delinsGTT MANE Select	NP_808592.2:n.785+174_785+176delinsGTT
NM_001127505.3:c.767+174_767+176delinsGTT	NP_001120977.1:n.767+174_767+176delinsGTT
NM_001363743.2:c.590+174_590+176delinsGTT	NP_001350672.1:n.590+174_590+176delinsGTT
NM_004315.6:c.833+174_833+176delinsGTT	NP_004306.3:n.833+174_833+176delinsGTT