Canonical Allele Identifier: CA1768020003
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061441G= , CM000670.2:g.18061441G= GRCh38
NC_000008.10:g.17918950G= , CM000670.1:g.17918950G= GRCh37
NC_000008.9:g.17963230G= NCBI36
NG_008985.1:g.28558C=
NG_008985.2:g.28558C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381733.9:c.769C= ENSP00000371152.4:p.Leu257=
ENST00000517409.2:n.689C=
ENST00000518746.2:n.2407C=
ENST00000519545.6:n.738C=
ENST00000520781.6:c.646C= ENSP00000427751.1:p.Leu216=
ENST00000521542.2:n.29C=
ENST00000635756.1:c.134C=
ENST00000635944.1:c.*557C= ENSP00000490195.1:n.*557C=
ENST00000635998.1:c.721C= ENSP00000490506.1:p.Leu241=
ENST00000636009.1:c.578C= ENSP00000489988.1:n.578C=
ENST00000636033.1:c.*557C= ENSP00000489617.1:n.*557C=
ENST00000636050.1:c.*564C= ENSP00000490562.1:n.*564C=
ENST00000636128.1:c.400C= ENSP00000489789.1:p.Leu134=
ENST00000636160.1:c.*613C= ENSP00000489651.1:n.*613C=
ENST00000636171.1:c.664C= ENSP00000489761.1:p.Leu222=
ENST00000636455.1:c.769C= ENSP00000490502.1:p.Leu257=
ENST00000636494.1:c.*501C= ENSP00000490388.1:n.*501C=
ENST00000636563.1:n.383C=
ENST00000636577.1:c.661C= ENSP00000490027.1:p.Leu221=
ENST00000636691.1:c.526C= ENSP00000490725.1:p.Leu176=
ENST00000636701.1:c.*372C= ENSP00000489800.1:n.*372C=
ENST00000636815.1:c.638C=
ENST00000636920.1:c.*557C= ENSP00000490437.1:n.*557C=
ENST00000636997.1:c.634C= ENSP00000490093.1:p.Leu212=
ENST00000637013.1:c.*1089C= ENSP00000490596.1:n.*1089C=
ENST00000637014.1:n.1128C=
ENST00000637095.1:c.*501C= ENSP00000490415.1:n.*501C=
ENST00000637244.1:c.*1239C= ENSP00000490188.1:n.*1239C=
ENST00000637343.1:n.2158C=
ENST00000637429.1:c.*933C= ENSP00000490522.1:n.*933C=
ENST00000637484.1:c.*683C= ENSP00000490837.1:n.*683C=
ENST00000637528.1:c.658C= ENSP00000490801.1:p.Leu220=
ENST00000637609.1:n.3442C=
ENST00000637636.1:c.715C= ENSP00000490112.1:p.Leu239=
ENST00000637790.2:c.721C= MANE Select ENSP00000490272.1:p.Leu241=
ENST00000637857.1:n.1087C=
ENST00000637922.1:c.526C= ENSP00000490071.1:p.Leu176=
ENST00000637991.1:c.694C= ENSP00000489901.1:p.Leu232=
ENST00000638028.1:n.938C=
ENST00000638069.1:n.1542C=
ENST00000262097.10:c.721C= ENSP00000262097.6:p.Leu241=
ENST00000314146.10:c.703C= ENSP00000326970.10:p.Leu235=
ENST00000381733.8:c.769C= ENSP00000371152.4:p.Leu257=
ENST00000518746.1:n.538C=
ENST00000519468.5:n.550C=
ENST00000520781.5:c.646C= ENSP00000427751.1:p.Leu216=
ENST00000521542.1:n.434C=
NM_001127505.1:c.703C= NP_001120977.1:p.Leu235=
NM_001127505.2:c.703C= NP_001120977.1:p.Leu235=
NM_004315.4:c.769C= NP_004306.3:p.Leu257=
NM_004315.5:c.769C= NP_004306.3:p.Leu257=
NM_177924.3:c.721C= NP_808592.2:p.Leu241=
NM_177924.4:c.721C= NP_808592.2:p.Leu241=
XM_005273504.2:c.655C= XP_005273561.1:p.Leu219=
NM_001363743.1:c.526C= NP_001350672.1:p.Leu176=
XM_005273504.3:c.655C= XP_005273561.1:p.Leu219=
NM_177924.5:c.721C= MANE Select NP_808592.2:p.Leu241=
NM_001127505.3:c.703C= NP_001120977.1:p.Leu235=
NM_001363743.2:c.526C= NP_001350672.1:p.Leu176=
NM_004315.6:c.769C= NP_004306.3:p.Leu257=