Canonical Allele Identifier: CA1768025407
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064518T= , CM000670.2:g.18064518T= GRCh38
NC_000008.10:g.17922027T= , CM000670.1:g.17922027T= GRCh37
NC_000008.9:g.17966307T= NCBI36
NG_008985.1:g.25481A=
NG_008985.2:g.25481A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.444A= ENSP00000371152.4:p.Ser148=
ENST00000519545.6:n.413A=
ENST00000520781.6:c.383-1288A= ENSP00000427751.1:n.383-1288A=
ENST00000523593.6:c.*239A= ENSP00000490700.1:n.*239A=
ENST00000523744.2:n.4154A=
ENST00000635769.1:c.417A= ENSP00000490485.1:p.Ser139=
ENST00000635944.1:c.*232A= ENSP00000490195.1:n.*232A=
ENST00000635998.1:c.396A= ENSP00000490506.1:p.Ser132=
ENST00000636009.1:c.315-1288A= ENSP00000489988.1:n.315-1288A=
ENST00000636033.1:c.*232A= ENSP00000489617.1:n.*232A=
ENST00000636050.1:c.*239A= ENSP00000490562.1:n.*239A=
ENST00000636128.1:c.382+2702A= ENSP00000489789.1:n.382+2702A=
ENST00000636160.1:c.*288A= ENSP00000489651.1:n.*288A=
ENST00000636171.1:c.383-44A= ENSP00000489761.1:n.383-44A=
ENST00000636299.1:c.*167A= ENSP00000490202.1:n.*167A=
ENST00000636435.1:n.3168A=
ENST00000636455.1:c.444A= ENSP00000490502.1:p.Ser148=
ENST00000636494.1:c.*176A= ENSP00000490388.1:n.*176A=
ENST00000636563.1:n.58A=
ENST00000636577.1:c.383-47A= ENSP00000490027.1:n.383-47A=
ENST00000636691.1:c.201A= ENSP00000490725.1:p.Ser67=
ENST00000636701.1:c.*47A= ENSP00000489800.1:n.*47A=
ENST00000636815.1:c.313A=
ENST00000636823.1:c.201A= ENSP00000490798.1:p.Ser67=
ENST00000636828.1:n.3260A=
ENST00000636920.1:c.*232A= ENSP00000490437.1:n.*232A=
ENST00000636997.1:c.309A= ENSP00000490093.1:p.Ser103=
ENST00000637013.1:c.*608A= ENSP00000490596.1:n.*608A=
ENST00000637095.1:c.*176A= ENSP00000490415.1:n.*176A=
ENST00000637244.1:c.*914A= ENSP00000490188.1:n.*914A=
ENST00000637343.1:n.607A=
ENST00000637429.1:c.*608A= ENSP00000490522.1:n.*608A=
ENST00000637484.1:c.*420-1288A= ENSP00000490837.1:n.*420-1288A=
ENST00000637528.1:c.383-50A= ENSP00000490801.1:n.383-50A=
ENST00000637603.1:c.366A= ENSP00000489979.1:p.Ser122=
ENST00000637609.1:n.3117A=
ENST00000637636.1:c.390A= ENSP00000490112.1:p.Ser130=
ENST00000637638.1:c.396A= ENSP00000490774.1:p.Ser132=
ENST00000637718.1:c.201A= ENSP00000490133.1:p.Ser67=
ENST00000637790.2:c.396A= MANE Select ENSP00000490272.1:p.Ser132=
ENST00000637857.1:n.105-2095A=
ENST00000637922.1:c.201A= ENSP00000490071.1:p.Ser67=
ENST00000637991.1:c.431-1288A= ENSP00000489901.1:n.431-1288A=
ENST00000638069.1:n.452A=
ENST00000262097.10:c.396A= ENSP00000262097.6:p.Ser132=
ENST00000314146.10:c.378A= ENSP00000326970.10:p.Ser126=
ENST00000381733.8:c.444A= ENSP00000371152.4:p.Ser148=
ENST00000519468.5:n.389-2151A=
ENST00000519545.5:n.410A=
ENST00000520781.5:c.383-1288A= ENSP00000427751.1:n.383-1288A=
ENST00000523593.5:n.249A=
ENST00000523744.1:n.399A=
NM_001127505.1:c.378A= NP_001120977.1:p.Ser126=
NM_001127505.2:c.378A= NP_001120977.1:p.Ser126=
NM_004315.4:c.444A= NP_004306.3:p.Ser148=
NM_004315.5:c.444A= NP_004306.3:p.Ser148=
NM_177924.3:c.396A= NP_808592.2:p.Ser132=
NM_177924.4:c.396A= NP_808592.2:p.Ser132=
XM_005273504.2:c.330A= XP_005273561.1:p.Ser110=
NM_001363743.1:c.201A= NP_001350672.1:p.Ser67=
XM_005273504.3:c.330A= XP_005273561.1:p.Ser110=
NM_177924.5:c.396A= MANE Select NP_808592.2:p.Ser132=
NM_001127505.3:c.378A= NP_001120977.1:p.Ser126=
NM_001363743.2:c.201A= NP_001350672.1:p.Ser67=
NM_004315.6:c.444A= NP_004306.3:p.Ser148=