Canonical Allele Identifier: CA1768013037
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18057221A= , CM000670.2:g.18057221A= GRCh38
NC_000008.10:g.17914730A= , CM000670.1:g.17914730A= GRCh37
NC_000008.9:g.17959010A= NCBI36
NG_008985.1:g.32778T=
NG_008985.2:g.32778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.*313T= ENSP00000371152.4:n.*313T=
ENST00000518746.2:n.3187T=
ENST00000520781.6:c.*313T= ENSP00000427751.1:n.*313T=
ENST00000635756.1:c.914T=
ENST00000635944.1:c.*1337T= ENSP00000490195.1:n.*1337T=
ENST00000635998.1:c.*214T= ENSP00000490506.1:n.*214T=
ENST00000636009.1:c.1358T= ENSP00000489988.1:n.1358T=
ENST00000636033.1:c.*1337T= ENSP00000489617.1:n.*1337T=
ENST00000636050.1:c.*1344T= ENSP00000490562.1:n.*1344T=
ENST00000636128.1:c.*313T= ENSP00000489789.1:n.*313T=
ENST00000636160.1:c.*1393T= ENSP00000489651.1:n.*1393T=
ENST00000636171.1:c.*313T= ENSP00000489761.1:n.*313T=
ENST00000636455.1:c.*399T= ENSP00000490502.1:n.*399T=
ENST00000636494.1:c.*1281T= ENSP00000490388.1:n.*1281T=
ENST00000636563.1:n.1163T=
ENST00000636577.1:c.*313T= ENSP00000490027.1:n.*313T=
ENST00000636691.1:c.*313T= ENSP00000490725.1:n.*313T=
ENST00000636701.1:c.*1152T= ENSP00000489800.1:n.*1152T=
ENST00000636815.1:c.1418T=
ENST00000636920.1:c.*1337T= ENSP00000490437.1:n.*1337T=
ENST00000636997.1:c.*313T= ENSP00000490093.1:n.*313T=
ENST00000637013.1:c.*1869T= ENSP00000490596.1:n.*1869T=
ENST00000637014.1:n.1908T=
ENST00000637095.1:c.*1281T= ENSP00000490415.1:n.*1281T=
ENST00000637244.1:c.*2019T= ENSP00000490188.1:n.*2019T=
ENST00000637343.1:n.2938T=
ENST00000637429.1:c.*1713T= ENSP00000490522.1:n.*1713T=
ENST00000637484.1:c.*1463T= ENSP00000490837.1:n.*1463T=
ENST00000637528.1:c.*313T= ENSP00000490801.1:n.*313T=
ENST00000637609.1:n.4222T=
ENST00000637636.1:c.*313T= ENSP00000490112.1:n.*313T=
ENST00000637752.1:n.1943T=
ENST00000637790.2:c.*313T= MANE Select ENSP00000490272.1:n.*313T=
ENST00000637857.1:n.1867T=
ENST00000637922.1:c.*313T= ENSP00000490071.1:n.*313T=
ENST00000637991.1:c.*313T= ENSP00000489901.1:n.*313T=
ENST00000638028.1:n.1718T=
ENST00000638069.1:n.2322T=
ENST00000262097.10:c.*313T= ENSP00000262097.6:n.*313T=
ENST00000314146.10:c.*313T= ENSP00000326970.10:n.*313T=
ENST00000381733.8:c.*313T= ENSP00000371152.4:n.*313T=
ENST00000520781.5:c.*313T= ENSP00000427751.1:n.*313T=
NM_001127505.1:c.*313T= NP_001120977.1:n.*313T=
NM_001127505.2:c.*313T= NP_001120977.1:n.*313T=
NM_004315.4:c.*313T= NP_004306.3:n.*313T=
NM_004315.5:c.*313T= NP_004306.3:n.*313T=
NM_177924.3:c.*313T= NP_808592.2:n.*313T=
NM_177924.4:c.*313T= NP_808592.2:n.*313T=
XM_005273504.2:c.*313T= XP_005273561.1:n.*313T=
NM_001363743.1:c.*313T= NP_001350672.1:n.*313T=
XM_005273504.3:c.*313T= XP_005273561.1:n.*313T=
NM_177924.5:c.*313T= MANE Select NP_808592.2:n.*313T=
NM_001127505.3:c.*313T= NP_001120977.1:n.*313T=
NM_001363743.2:c.*313T= NP_001350672.1:n.*313T=
NM_004315.6:c.*313T= NP_004306.3:n.*313T=