Canonical Allele Identifier: CA1768019884
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061384T= , CM000670.2:g.18061384T= GRCh38
NC_000008.10:g.17918893T= , CM000670.1:g.17918893T= GRCh37
NC_000008.9:g.17963173T= NCBI36
NG_008985.1:g.28615A=
NG_008985.2:g.28615A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.826A= ENSP00000371152.4:p.Ser276=
ENST00000518746.2:n.2464A=
ENST00000520781.6:c.703A= ENSP00000427751.1:p.Ser235=
ENST00000521542.2:n.86A=
ENST00000635756.1:c.191A=
ENST00000635944.1:c.*614A= ENSP00000490195.1:n.*614A=
ENST00000635998.1:c.778A= ENSP00000490506.1:p.Ser260=
ENST00000636009.1:c.635A= ENSP00000489988.1:n.635A=
ENST00000636033.1:c.*614A= ENSP00000489617.1:n.*614A=
ENST00000636050.1:c.*621A= ENSP00000490562.1:n.*621A=
ENST00000636128.1:c.457A= ENSP00000489789.1:p.Ser153=
ENST00000636160.1:c.*670A= ENSP00000489651.1:n.*670A=
ENST00000636171.1:c.721A= ENSP00000489761.1:p.Ser241=
ENST00000636455.1:c.826A= ENSP00000490502.1:p.Ser276=
ENST00000636494.1:c.*558A= ENSP00000490388.1:n.*558A=
ENST00000636563.1:n.440A=
ENST00000636577.1:c.718A= ENSP00000490027.1:p.Ser240=
ENST00000636691.1:c.583A= ENSP00000490725.1:p.Ser195=
ENST00000636701.1:c.*429A= ENSP00000489800.1:n.*429A=
ENST00000636815.1:c.695A=
ENST00000636920.1:c.*614A= ENSP00000490437.1:n.*614A=
ENST00000636997.1:c.691A= ENSP00000490093.1:p.Ser231=
ENST00000637013.1:c.*1146A= ENSP00000490596.1:n.*1146A=
ENST00000637014.1:n.1185A=
ENST00000637095.1:c.*558A= ENSP00000490415.1:n.*558A=
ENST00000637244.1:c.*1296A= ENSP00000490188.1:n.*1296A=
ENST00000637343.1:n.2215A=
ENST00000637429.1:c.*990A= ENSP00000490522.1:n.*990A=
ENST00000637484.1:c.*740A= ENSP00000490837.1:n.*740A=
ENST00000637528.1:c.715A= ENSP00000490801.1:p.Ser239=
ENST00000637609.1:n.3499A=
ENST00000637636.1:c.772A= ENSP00000490112.1:p.Ser258=
ENST00000637790.2:c.778A= MANE Select ENSP00000490272.1:p.Ser260=
ENST00000637857.1:n.1144A=
ENST00000637922.1:c.583A= ENSP00000490071.1:p.Ser195=
ENST00000637991.1:c.751A= ENSP00000489901.1:p.Ser251=
ENST00000638028.1:n.995A=
ENST00000638069.1:n.1599A=
ENST00000262097.10:c.778A= ENSP00000262097.6:p.Ser260=
ENST00000314146.10:c.760A= ENSP00000326970.10:p.Ser254=
ENST00000381733.8:c.826A= ENSP00000371152.4:p.Ser276=
ENST00000519468.5:n.607A=
ENST00000520781.5:c.703A= ENSP00000427751.1:p.Ser235=
ENST00000521542.1:n.491A=
NM_001127505.1:c.760A= NP_001120977.1:p.Ser254=
NM_001127505.2:c.760A= NP_001120977.1:p.Ser254=
NM_004315.4:c.826A= NP_004306.3:p.Ser276=
NM_004315.5:c.826A= NP_004306.3:p.Ser276=
NM_177924.3:c.778A= NP_808592.2:p.Ser260=
NM_177924.4:c.778A= NP_808592.2:p.Ser260=
XM_005273504.2:c.712A= XP_005273561.1:p.Ser238=
NM_001363743.1:c.583A= NP_001350672.1:p.Ser195=
XM_005273504.3:c.712A= XP_005273561.1:p.Ser238=
NM_177924.5:c.778A= MANE Select NP_808592.2:p.Ser260=
NM_001127505.3:c.760A= NP_001120977.1:p.Ser254=
NM_001363743.2:c.583A= NP_001350672.1:p.Ser195=
NM_004315.6:c.826A= NP_004306.3:p.Ser276=