Canonical Allele Identifier: CA2686314998

Gene: ASAH1

Linked Data

• gnomAD v4: 8-18061281-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061281C>A , CM000670.2:g.18061281C>A	GRCh38
NC_000008.10:g.17918790C>A , CM000670.1:g.17918790C>A	GRCh37
NC_000008.9:g.17963070C>A	NCBI36
NG_008985.1:g.28718G>T
NG_008985.2:g.28718G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381733.9:c.833+96G>T	ENSP00000371152.4:n.833+96G>T
ENST00000518746.2:n.2471+96G>T
ENST00000520781.6:c.710+96G>T	ENSP00000427751.1:n.710+96G>T
ENST00000521542.2:n.189G>T
ENST00000635756.1:c.198+96G>T
ENST00000635944.1:c.*621+96G>T	ENSP00000490195.1:n.*621+96G>T
ENST00000635998.1:c.785+96G>T	ENSP00000490506.1:n.785+96G>T
ENST00000636009.1:c.642+96G>T	ENSP00000489988.1:n.642+96G>T
ENST00000636033.1:c.*621+96G>T	ENSP00000489617.1:n.*621+96G>T
ENST00000636050.1:c.*628+96G>T	ENSP00000490562.1:n.*628+96G>T
ENST00000636128.1:c.464+96G>T	ENSP00000489789.1:n.464+96G>T
ENST00000636160.1:c.*677+96G>T	ENSP00000489651.1:n.*677+96G>T
ENST00000636171.1:c.728+96G>T	ENSP00000489761.1:n.728+96G>T
ENST00000636455.1:c.833+96G>T	ENSP00000490502.1:n.833+96G>T
ENST00000636494.1:c.*565+96G>T	ENSP00000490388.1:n.*565+96G>T
ENST00000636563.1:n.447+96G>T
ENST00000636577.1:c.725+96G>T	ENSP00000490027.1:n.725+96G>T
ENST00000636691.1:c.590+96G>T	ENSP00000490725.1:n.590+96G>T
ENST00000636701.1:c.*436+96G>T	ENSP00000489800.1:n.*436+96G>T
ENST00000636815.1:c.702+96G>T
ENST00000636920.1:c.*621+96G>T	ENSP00000490437.1:n.*621+96G>T
ENST00000636997.1:c.698+96G>T	ENSP00000490093.1:n.698+96G>T
ENST00000637013.1:c.*1153+96G>T	ENSP00000490596.1:n.*1153+96G>T
ENST00000637014.1:n.1192+96G>T
ENST00000637095.1:c.*565+96G>T	ENSP00000490415.1:n.*565+96G>T
ENST00000637244.1:c.*1303+96G>T	ENSP00000490188.1:n.*1303+96G>T
ENST00000637343.1:n.2222+96G>T
ENST00000637429.1:c.*997+96G>T	ENSP00000490522.1:n.*997+96G>T
ENST00000637484.1:c.*747+96G>T	ENSP00000490837.1:n.*747+96G>T
ENST00000637528.1:c.722+96G>T	ENSP00000490801.1:n.722+96G>T
ENST00000637609.1:n.3506+96G>T
ENST00000637636.1:c.779+96G>T	ENSP00000490112.1:n.779+96G>T
ENST00000637790.2:c.785+96G>T MANE Select	ENSP00000490272.1:n.785+96G>T
ENST00000637857.1:n.1151+96G>T
ENST00000637922.1:c.590+96G>T	ENSP00000490071.1:n.590+96G>T
ENST00000637991.1:c.758+96G>T	ENSP00000489901.1:n.758+96G>T
ENST00000638028.1:n.1002+96G>T
ENST00000638069.1:n.1606+96G>T
ENST00000262097.10:c.785+96G>T	ENSP00000262097.6:n.785+96G>T
ENST00000314146.10:c.767+96G>T	ENSP00000326970.10:n.767+96G>T
ENST00000381733.8:c.833+96G>T	ENSP00000371152.4:n.833+96G>T
ENST00000519468.5:n.614+96G>T
ENST00000520781.5:c.710+96G>T	ENSP00000427751.1:n.710+96G>T
ENST00000521542.1:n.498+96G>T
NM_001127505.1:c.767+96G>T	NP_001120977.1:n.767+96G>T
NM_001127505.2:c.767+96G>T	NP_001120977.1:n.767+96G>T
NM_004315.4:c.833+96G>T	NP_004306.3:n.833+96G>T
NM_004315.5:c.833+96G>T	NP_004306.3:n.833+96G>T
NM_177924.3:c.785+96G>T	NP_808592.2:n.785+96G>T
NM_177924.4:c.785+96G>T	NP_808592.2:n.785+96G>T
XM_005273504.2:c.719+96G>T	XP_005273561.1:n.719+96G>T
NM_001363743.1:c.590+96G>T	NP_001350672.1:n.590+96G>T
XM_005273504.3:c.719+96G>T	XP_005273561.1:n.719+96G>T
NM_177924.5:c.785+96G>T MANE Select	NP_808592.2:n.785+96G>T
NM_001127505.3:c.767+96G>T	NP_001120977.1:n.767+96G>T
NM_001363743.2:c.590+96G>T	NP_001350672.1:n.590+96G>T
NM_004315.6:c.833+96G>T	NP_004306.3:n.833+96G>T