Canonical Allele Identifier: CA1768019699

Gene: ASAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061306_18061307delinsCA , CM000670.2:g.18061306_18061307delinsCA	GRCh38
NC_000008.10:g.17918815_17918816delinsCA , CM000670.1:g.17918815_17918816delinsCA	GRCh37
NC_000008.9:g.17963095_17963096delinsCA	NCBI36
NG_008985.1:g.28692_28693delinsTG
NG_008985.2:g.28692_28693delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.833+70_833+71delinsTG	ENSP00000371152.4:n.833+70_833+71delinsTG
ENST00000518746.2:n.2471+70_2471+71delinsTG
ENST00000520781.6:c.710+70_710+71delinsTG	ENSP00000427751.1:n.710+70_710+71delinsTG
ENST00000521542.2:n.163_164delinsTG
ENST00000635756.1:c.198+70_198+71delinsTG
ENST00000635944.1:c.*621+70_*621+71delinsTG	ENSP00000490195.1:n.*621+70_*621+71delinsTG
ENST00000635998.1:c.785+70_785+71delinsTG	ENSP00000490506.1:n.785+70_785+71delinsTG
ENST00000636009.1:c.642+70_642+71delinsTG	ENSP00000489988.1:n.642+70_642+71delinsTG
ENST00000636033.1:c.*621+70_*621+71delinsTG	ENSP00000489617.1:n.*621+70_*621+71delinsTG
ENST00000636050.1:c.*628+70_*628+71delinsTG	ENSP00000490562.1:n.*628+70_*628+71delinsTG
ENST00000636128.1:c.464+70_464+71delinsTG	ENSP00000489789.1:n.464+70_464+71delinsTG
ENST00000636160.1:c.*677+70_*677+71delinsTG	ENSP00000489651.1:n.*677+70_*677+71delinsTG
ENST00000636171.1:c.728+70_728+71delinsTG	ENSP00000489761.1:n.728+70_728+71delinsTG
ENST00000636455.1:c.833+70_833+71delinsTG	ENSP00000490502.1:n.833+70_833+71delinsTG
ENST00000636494.1:c.*565+70_*565+71delinsTG	ENSP00000490388.1:n.*565+70_*565+71delinsTG
ENST00000636563.1:n.447+70_447+71delinsTG
ENST00000636577.1:c.725+70_725+71delinsTG	ENSP00000490027.1:n.725+70_725+71delinsTG
ENST00000636691.1:c.590+70_590+71delinsTG	ENSP00000490725.1:n.590+70_590+71delinsTG
ENST00000636701.1:c.*436+70_*436+71delinsTG	ENSP00000489800.1:n.*436+70_*436+71delinsTG
ENST00000636815.1:c.702+70_702+71delinsTG
ENST00000636920.1:c.*621+70_*621+71delinsTG	ENSP00000490437.1:n.*621+70_*621+71delinsTG
ENST00000636997.1:c.698+70_698+71delinsTG	ENSP00000490093.1:n.698+70_698+71delinsTG
ENST00000637013.1:c.*1153+70_*1153+71delinsTG	ENSP00000490596.1:n.*1153+70_*1153+71delinsTG
ENST00000637014.1:n.1192+70_1192+71delinsTG
ENST00000637095.1:c.*565+70_*565+71delinsTG	ENSP00000490415.1:n.*565+70_*565+71delinsTG
ENST00000637244.1:c.*1303+70_*1303+71delinsTG	ENSP00000490188.1:n.*1303+70_*1303+71delinsTG
ENST00000637343.1:n.2222+70_2222+71delinsTG
ENST00000637429.1:c.*997+70_*997+71delinsTG	ENSP00000490522.1:n.*997+70_*997+71delinsTG
ENST00000637484.1:c.*747+70_*747+71delinsTG	ENSP00000490837.1:n.*747+70_*747+71delinsTG
ENST00000637528.1:c.722+70_722+71delinsTG	ENSP00000490801.1:n.722+70_722+71delinsTG
ENST00000637609.1:n.3506+70_3506+71delinsTG
ENST00000637636.1:c.779+70_779+71delinsTG	ENSP00000490112.1:n.779+70_779+71delinsTG
ENST00000637790.2:c.785+70_785+71delinsTG MANE Select	ENSP00000490272.1:n.785+70_785+71delinsTG
ENST00000637857.1:n.1151+70_1151+71delinsTG
ENST00000637922.1:c.590+70_590+71delinsTG	ENSP00000490071.1:n.590+70_590+71delinsTG
ENST00000637991.1:c.758+70_758+71delinsTG	ENSP00000489901.1:n.758+70_758+71delinsTG
ENST00000638028.1:n.1002+70_1002+71delinsTG
ENST00000638069.1:n.1606+70_1606+71delinsTG
ENST00000262097.10:c.785+70_785+71delinsTG	ENSP00000262097.6:n.785+70_785+71delinsTG
ENST00000314146.10:c.767+70_767+71delinsTG	ENSP00000326970.10:n.767+70_767+71delinsTG
ENST00000381733.8:c.833+70_833+71delinsTG	ENSP00000371152.4:n.833+70_833+71delinsTG
ENST00000519468.5:n.614+70_614+71delinsTG
ENST00000520781.5:c.710+70_710+71delinsTG	ENSP00000427751.1:n.710+70_710+71delinsTG
ENST00000521542.1:n.498+70_498+71delinsTG
NM_001127505.1:c.767+70_767+71delinsTG	NP_001120977.1:n.767+70_767+71delinsTG
NM_001127505.2:c.767+70_767+71delinsTG	NP_001120977.1:n.767+70_767+71delinsTG
NM_004315.4:c.833+70_833+71delinsTG	NP_004306.3:n.833+70_833+71delinsTG
NM_004315.5:c.833+70_833+71delinsTG	NP_004306.3:n.833+70_833+71delinsTG
NM_177924.3:c.785+70_785+71delinsTG	NP_808592.2:n.785+70_785+71delinsTG
NM_177924.4:c.785+70_785+71delinsTG	NP_808592.2:n.785+70_785+71delinsTG
XM_005273504.2:c.719+70_719+71delinsTG	XP_005273561.1:n.719+70_719+71delinsTG
NM_001363743.1:c.590+70_590+71delinsTG	NP_001350672.1:n.590+70_590+71delinsTG
XM_005273504.3:c.719+70_719+71delinsTG	XP_005273561.1:n.719+70_719+71delinsTG
NM_177924.5:c.785+70_785+71delinsTG MANE Select	NP_808592.2:n.785+70_785+71delinsTG
NM_001127505.3:c.767+70_767+71delinsTG	NP_001120977.1:n.767+70_767+71delinsTG
NM_001363743.2:c.590+70_590+71delinsTG	NP_001350672.1:n.590+70_590+71delinsTG
NM_004315.6:c.833+70_833+71delinsTG	NP_004306.3:n.833+70_833+71delinsTG