Canonical Allele Identifier: CA1768019915
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061400T= , CM000670.2:g.18061400T= GRCh38
NC_000008.10:g.17918909T= , CM000670.1:g.17918909T= GRCh37
NC_000008.9:g.17963189T= NCBI36
NG_008985.1:g.28599A=
NG_008985.2:g.28599A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.810A= ENSP00000371152.4:p.Arg270=
ENST00000517409.2:n.730A=
ENST00000518746.2:n.2448A=
ENST00000520781.6:c.687A= ENSP00000427751.1:p.Arg229=
ENST00000521542.2:n.70A=
ENST00000635756.1:c.175A=
ENST00000635944.1:c.*598A= ENSP00000490195.1:n.*598A=
ENST00000635998.1:c.762A= ENSP00000490506.1:p.Arg254=
ENST00000636009.1:c.619A= ENSP00000489988.1:n.619A=
ENST00000636033.1:c.*598A= ENSP00000489617.1:n.*598A=
ENST00000636050.1:c.*605A= ENSP00000490562.1:n.*605A=
ENST00000636128.1:c.441A= ENSP00000489789.1:p.Arg147=
ENST00000636160.1:c.*654A= ENSP00000489651.1:n.*654A=
ENST00000636171.1:c.705A= ENSP00000489761.1:p.Arg235=
ENST00000636455.1:c.810A= ENSP00000490502.1:p.Arg270=
ENST00000636494.1:c.*542A= ENSP00000490388.1:n.*542A=
ENST00000636563.1:n.424A=
ENST00000636577.1:c.702A= ENSP00000490027.1:p.Arg234=
ENST00000636691.1:c.567A= ENSP00000490725.1:p.Arg189=
ENST00000636701.1:c.*413A= ENSP00000489800.1:n.*413A=
ENST00000636815.1:c.679A=
ENST00000636920.1:c.*598A= ENSP00000490437.1:n.*598A=
ENST00000636997.1:c.675A= ENSP00000490093.1:p.Arg225=
ENST00000637013.1:c.*1130A= ENSP00000490596.1:n.*1130A=
ENST00000637014.1:n.1169A=
ENST00000637095.1:c.*542A= ENSP00000490415.1:n.*542A=
ENST00000637244.1:c.*1280A= ENSP00000490188.1:n.*1280A=
ENST00000637343.1:n.2199A=
ENST00000637429.1:c.*974A= ENSP00000490522.1:n.*974A=
ENST00000637484.1:c.*724A= ENSP00000490837.1:n.*724A=
ENST00000637528.1:c.699A= ENSP00000490801.1:p.Arg233=
ENST00000637609.1:n.3483A=
ENST00000637636.1:c.756A= ENSP00000490112.1:p.Arg252=
ENST00000637790.2:c.762A= MANE Select ENSP00000490272.1:p.Arg254=
ENST00000637857.1:n.1128A=
ENST00000637922.1:c.567A= ENSP00000490071.1:p.Arg189=
ENST00000637991.1:c.735A= ENSP00000489901.1:p.Arg245=
ENST00000638028.1:n.979A=
ENST00000638069.1:n.1583A=
ENST00000262097.10:c.762A= ENSP00000262097.6:p.Arg254=
ENST00000314146.10:c.744A= ENSP00000326970.10:p.Arg248=
ENST00000381733.8:c.810A= ENSP00000371152.4:p.Arg270=
ENST00000518746.1:n.579A=
ENST00000519468.5:n.591A=
ENST00000520781.5:c.687A= ENSP00000427751.1:p.Arg229=
ENST00000521542.1:n.475A=
NM_001127505.1:c.744A= NP_001120977.1:p.Arg248=
NM_001127505.2:c.744A= NP_001120977.1:p.Arg248=
NM_004315.4:c.810A= NP_004306.3:p.Arg270=
NM_004315.5:c.810A= NP_004306.3:p.Arg270=
NM_177924.3:c.762A= NP_808592.2:p.Arg254=
NM_177924.4:c.762A= NP_808592.2:p.Arg254=
XM_005273504.2:c.696A= XP_005273561.1:p.Arg232=
NM_001363743.1:c.567A= NP_001350672.1:p.Arg189=
XM_005273504.3:c.696A= XP_005273561.1:p.Arg232=
NM_177924.5:c.762A= MANE Select NP_808592.2:p.Arg254=
NM_001127505.3:c.744A= NP_001120977.1:p.Arg248=
NM_001363743.2:c.567A= NP_001350672.1:p.Arg189=
NM_004315.6:c.810A= NP_004306.3:p.Arg270=