Canonical Allele Identifier: CA1768019959

Gene: ASAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061416A= , CM000670.2:g.18061416A=	GRCh38
NC_000008.10:g.17918925A= , CM000670.1:g.17918925A=	GRCh37
NC_000008.9:g.17963205A=	NCBI36
NG_008985.1:g.28583T=
NG_008985.2:g.28583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.794T=	ENSP00000371152.4:p.Ile265=
ENST00000517409.2:n.714T=
ENST00000518746.2:n.2432T=
ENST00000519545.6:n.763T=
ENST00000520781.6:c.671T=	ENSP00000427751.1:p.Ile224=
ENST00000521542.2:n.54T=
ENST00000635756.1:c.159T=
ENST00000635944.1:c.*582T=	ENSP00000490195.1:n.*582T=
ENST00000635998.1:c.746T=	ENSP00000490506.1:p.Ile249=
ENST00000636009.1:c.603T=	ENSP00000489988.1:n.603T=
ENST00000636033.1:c.*582T=	ENSP00000489617.1:n.*582T=
ENST00000636050.1:c.*589T=	ENSP00000490562.1:n.*589T=
ENST00000636128.1:c.425T=	ENSP00000489789.1:p.Ile142=
ENST00000636160.1:c.*638T=	ENSP00000489651.1:n.*638T=
ENST00000636171.1:c.689T=	ENSP00000489761.1:p.Ile230=
ENST00000636455.1:c.794T=	ENSP00000490502.1:p.Ile265=
ENST00000636494.1:c.*526T=	ENSP00000490388.1:n.*526T=
ENST00000636563.1:n.408T=
ENST00000636577.1:c.686T=	ENSP00000490027.1:p.Ile229=
ENST00000636691.1:c.551T=	ENSP00000490725.1:p.Ile184=
ENST00000636701.1:c.*397T=	ENSP00000489800.1:n.*397T=
ENST00000636815.1:c.663T=
ENST00000636920.1:c.*582T=	ENSP00000490437.1:n.*582T=
ENST00000636997.1:c.659T=	ENSP00000490093.1:p.Ile220=
ENST00000637013.1:c.*1114T=	ENSP00000490596.1:n.*1114T=
ENST00000637014.1:n.1153T=
ENST00000637095.1:c.*526T=	ENSP00000490415.1:n.*526T=
ENST00000637244.1:c.*1264T=	ENSP00000490188.1:n.*1264T=
ENST00000637343.1:n.2183T=
ENST00000637429.1:c.*958T=	ENSP00000490522.1:n.*958T=
ENST00000637484.1:c.*708T=	ENSP00000490837.1:n.*708T=
ENST00000637528.1:c.683T=	ENSP00000490801.1:p.Ile228=
ENST00000637609.1:n.3467T=
ENST00000637636.1:c.740T=	ENSP00000490112.1:p.Ile247=
ENST00000637790.2:c.746T= MANE Select	ENSP00000490272.1:p.Ile249=
ENST00000637857.1:n.1112T=
ENST00000637922.1:c.551T=	ENSP00000490071.1:p.Ile184=
ENST00000637991.1:c.719T=	ENSP00000489901.1:p.Ile240=
ENST00000638028.1:n.963T=
ENST00000638069.1:n.1567T=
ENST00000262097.10:c.746T=	ENSP00000262097.6:p.Ile249=
ENST00000314146.10:c.728T=	ENSP00000326970.10:p.Ile243=
ENST00000381733.8:c.794T=	ENSP00000371152.4:p.Ile265=
ENST00000518746.1:n.563T=
ENST00000519468.5:n.575T=
ENST00000520781.5:c.671T=	ENSP00000427751.1:p.Ile224=
ENST00000521542.1:n.459T=
NM_001127505.1:c.728T=	NP_001120977.1:p.Ile243=
NM_001127505.2:c.728T=	NP_001120977.1:p.Ile243=
NM_004315.4:c.794T=	NP_004306.3:p.Ile265=
NM_004315.5:c.794T=	NP_004306.3:p.Ile265=
NM_177924.3:c.746T=	NP_808592.2:p.Ile249=
NM_177924.4:c.746T=	NP_808592.2:p.Ile249=
XM_005273504.2:c.680T=	XP_005273561.1:p.Ile227=
NM_001363743.1:c.551T=	NP_001350672.1:p.Ile184=
XM_005273504.3:c.680T=	XP_005273561.1:p.Ile227=
NM_177924.5:c.746T= MANE Select	NP_808592.2:p.Ile249=
NM_001127505.3:c.728T=	NP_001120977.1:p.Ile243=
NM_001363743.2:c.551T=	NP_001350672.1:p.Ile184=
NM_004315.6:c.794T=	NP_004306.3:p.Ile265=