Canonical Allele Identifier: CA1768013145
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18057321A= , CM000670.2:g.18057321A= GRCh38
NC_000008.10:g.17914830A= , CM000670.1:g.17914830A= GRCh37
NC_000008.9:g.17959110A= NCBI36
NG_008985.1:g.32678T=
NG_008985.2:g.32678T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.*213T= ENSP00000371152.4:n.*213T=
ENST00000518746.2:n.3087T=
ENST00000520781.6:c.*213T= ENSP00000427751.1:n.*213T=
ENST00000635756.1:c.814T=
ENST00000635944.1:c.*1237T= ENSP00000490195.1:n.*1237T=
ENST00000635998.1:c.*114T= ENSP00000490506.1:n.*114T=
ENST00000636009.1:c.1258T= ENSP00000489988.1:n.1258T=
ENST00000636033.1:c.*1237T= ENSP00000489617.1:n.*1237T=
ENST00000636050.1:c.*1244T= ENSP00000490562.1:n.*1244T=
ENST00000636128.1:c.*213T= ENSP00000489789.1:n.*213T=
ENST00000636160.1:c.*1293T= ENSP00000489651.1:n.*1293T=
ENST00000636171.1:c.*213T= ENSP00000489761.1:n.*213T=
ENST00000636455.1:c.*299T= ENSP00000490502.1:n.*299T=
ENST00000636494.1:c.*1181T= ENSP00000490388.1:n.*1181T=
ENST00000636563.1:n.1063T=
ENST00000636577.1:c.*213T= ENSP00000490027.1:n.*213T=
ENST00000636691.1:c.*213T= ENSP00000490725.1:n.*213T=
ENST00000636701.1:c.*1052T= ENSP00000489800.1:n.*1052T=
ENST00000636815.1:c.1318T=
ENST00000636920.1:c.*1237T= ENSP00000490437.1:n.*1237T=
ENST00000636997.1:c.*213T= ENSP00000490093.1:n.*213T=
ENST00000637013.1:c.*1769T= ENSP00000490596.1:n.*1769T=
ENST00000637014.1:n.1808T=
ENST00000637095.1:c.*1181T= ENSP00000490415.1:n.*1181T=
ENST00000637244.1:c.*1919T= ENSP00000490188.1:n.*1919T=
ENST00000637343.1:n.2838T=
ENST00000637429.1:c.*1613T= ENSP00000490522.1:n.*1613T=
ENST00000637484.1:c.*1363T= ENSP00000490837.1:n.*1363T=
ENST00000637528.1:c.*213T= ENSP00000490801.1:n.*213T=
ENST00000637609.1:n.4122T=
ENST00000637636.1:c.*213T= ENSP00000490112.1:n.*213T=
ENST00000637752.1:n.1843T=
ENST00000637790.2:c.*213T= MANE Select ENSP00000490272.1:n.*213T=
ENST00000637857.1:n.1767T=
ENST00000637922.1:c.*213T= ENSP00000490071.1:n.*213T=
ENST00000637991.1:c.*213T= ENSP00000489901.1:n.*213T=
ENST00000638028.1:n.1618T=
ENST00000638069.1:n.2222T=
ENST00000262097.10:c.*213T= ENSP00000262097.6:n.*213T=
ENST00000314146.10:c.*213T= ENSP00000326970.10:n.*213T=
ENST00000381733.8:c.*213T= ENSP00000371152.4:n.*213T=
ENST00000520781.5:c.*213T= ENSP00000427751.1:n.*213T=
NM_001127505.1:c.*213T= NP_001120977.1:n.*213T=
NM_001127505.2:c.*213T= NP_001120977.1:n.*213T=
NM_004315.4:c.*213T= NP_004306.3:n.*213T=
NM_004315.5:c.*213T= NP_004306.3:n.*213T=
NM_177924.3:c.*213T= NP_808592.2:n.*213T=
NM_177924.4:c.*213T= NP_808592.2:n.*213T=
XM_005273504.2:c.*213T= XP_005273561.1:n.*213T=
NM_001363743.1:c.*213T= NP_001350672.1:n.*213T=
XM_005273504.3:c.*213T= XP_005273561.1:n.*213T=
NM_177924.5:c.*213T= MANE Select NP_808592.2:n.*213T=
NM_001127505.3:c.*213T= NP_001120977.1:n.*213T=
NM_001363743.2:c.*213T= NP_001350672.1:n.*213T=
NM_004315.6:c.*213T= NP_004306.3:n.*213T=