Canonical Allele Identifier: CA1768019951
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061413C= , CM000670.2:g.18061413C= GRCh38
NC_000008.10:g.17918922C= , CM000670.1:g.17918922C= GRCh37
NC_000008.9:g.17963202C= NCBI36
NG_008985.1:g.28586G=
NG_008985.2:g.28586G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.797G= ENSP00000371152.4:p.Gly266=
ENST00000517409.2:n.717G=
ENST00000518746.2:n.2435G=
ENST00000519545.6:n.766G=
ENST00000520781.6:c.674G= ENSP00000427751.1:p.Gly225=
ENST00000521542.2:n.57G=
ENST00000635756.1:c.162G=
ENST00000635944.1:c.*585G= ENSP00000490195.1:n.*585G=
ENST00000635998.1:c.749G= ENSP00000490506.1:p.Gly250=
ENST00000636009.1:c.606G= ENSP00000489988.1:n.606G=
ENST00000636033.1:c.*585G= ENSP00000489617.1:n.*585G=
ENST00000636050.1:c.*592G= ENSP00000490562.1:n.*592G=
ENST00000636128.1:c.428G= ENSP00000489789.1:p.Gly143=
ENST00000636160.1:c.*641G= ENSP00000489651.1:n.*641G=
ENST00000636171.1:c.692G= ENSP00000489761.1:p.Gly231=
ENST00000636455.1:c.797G= ENSP00000490502.1:p.Gly266=
ENST00000636494.1:c.*529G= ENSP00000490388.1:n.*529G=
ENST00000636563.1:n.411G=
ENST00000636577.1:c.689G= ENSP00000490027.1:p.Gly230=
ENST00000636691.1:c.554G= ENSP00000490725.1:p.Gly185=
ENST00000636701.1:c.*400G= ENSP00000489800.1:n.*400G=
ENST00000636815.1:c.666G=
ENST00000636920.1:c.*585G= ENSP00000490437.1:n.*585G=
ENST00000636997.1:c.662G= ENSP00000490093.1:p.Gly221=
ENST00000637013.1:c.*1117G= ENSP00000490596.1:n.*1117G=
ENST00000637014.1:n.1156G=
ENST00000637095.1:c.*529G= ENSP00000490415.1:n.*529G=
ENST00000637244.1:c.*1267G= ENSP00000490188.1:n.*1267G=
ENST00000637343.1:n.2186G=
ENST00000637429.1:c.*961G= ENSP00000490522.1:n.*961G=
ENST00000637484.1:c.*711G= ENSP00000490837.1:n.*711G=
ENST00000637528.1:c.686G= ENSP00000490801.1:p.Gly229=
ENST00000637609.1:n.3470G=
ENST00000637636.1:c.743G= ENSP00000490112.1:p.Gly248=
ENST00000637790.2:c.749G= MANE Select ENSP00000490272.1:p.Gly250=
ENST00000637857.1:n.1115G=
ENST00000637922.1:c.554G= ENSP00000490071.1:p.Gly185=
ENST00000637991.1:c.722G= ENSP00000489901.1:p.Gly241=
ENST00000638028.1:n.966G=
ENST00000638069.1:n.1570G=
ENST00000262097.10:c.749G= ENSP00000262097.6:p.Gly250=
ENST00000314146.10:c.731G= ENSP00000326970.10:p.Gly244=
ENST00000381733.8:c.797G= ENSP00000371152.4:p.Gly266=
ENST00000518746.1:n.566G=
ENST00000519468.5:n.578G=
ENST00000520781.5:c.674G= ENSP00000427751.1:p.Gly225=
ENST00000521542.1:n.462G=
NM_001127505.1:c.731G= NP_001120977.1:p.Gly244=
NM_001127505.2:c.731G= NP_001120977.1:p.Gly244=
NM_004315.4:c.797G= NP_004306.3:p.Gly266=
NM_004315.5:c.797G= NP_004306.3:p.Gly266=
NM_177924.3:c.749G= NP_808592.2:p.Gly250=
NM_177924.4:c.749G= NP_808592.2:p.Gly250=
XM_005273504.2:c.683G= XP_005273561.1:p.Gly228=
NM_001363743.1:c.554G= NP_001350672.1:p.Gly185=
XM_005273504.3:c.683G= XP_005273561.1:p.Gly228=
NM_177924.5:c.749G= MANE Select NP_808592.2:p.Gly250=
NM_001127505.3:c.731G= NP_001120977.1:p.Gly244=
NM_001363743.2:c.554G= NP_001350672.1:p.Gly185=
NM_004315.6:c.797G= NP_004306.3:p.Gly266=