Canonical Allele Identifier: CA1768013122
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18057310T= , CM000670.2:g.18057310T= GRCh38
NC_000008.10:g.17914819T= , CM000670.1:g.17914819T= GRCh37
NC_000008.9:g.17959099T= NCBI36
NG_008985.1:g.32689A=
NG_008985.2:g.32689A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381733.9:c.*224A= ENSP00000371152.4:n.*224A=
ENST00000518746.2:n.3098A=
ENST00000520781.6:c.*224A= ENSP00000427751.1:n.*224A=
ENST00000635756.1:c.825A=
ENST00000635944.1:c.*1248A= ENSP00000490195.1:n.*1248A=
ENST00000635998.1:c.*125A= ENSP00000490506.1:n.*125A=
ENST00000636009.1:c.1269A= ENSP00000489988.1:n.1269A=
ENST00000636033.1:c.*1248A= ENSP00000489617.1:n.*1248A=
ENST00000636050.1:c.*1255A= ENSP00000490562.1:n.*1255A=
ENST00000636128.1:c.*224A= ENSP00000489789.1:n.*224A=
ENST00000636160.1:c.*1304A= ENSP00000489651.1:n.*1304A=
ENST00000636171.1:c.*224A= ENSP00000489761.1:n.*224A=
ENST00000636455.1:c.*310A= ENSP00000490502.1:n.*310A=
ENST00000636494.1:c.*1192A= ENSP00000490388.1:n.*1192A=
ENST00000636563.1:n.1074A=
ENST00000636577.1:c.*224A= ENSP00000490027.1:n.*224A=
ENST00000636691.1:c.*224A= ENSP00000490725.1:n.*224A=
ENST00000636701.1:c.*1063A= ENSP00000489800.1:n.*1063A=
ENST00000636815.1:c.1329A=
ENST00000636920.1:c.*1248A= ENSP00000490437.1:n.*1248A=
ENST00000636997.1:c.*224A= ENSP00000490093.1:n.*224A=
ENST00000637013.1:c.*1780A= ENSP00000490596.1:n.*1780A=
ENST00000637014.1:n.1819A=
ENST00000637095.1:c.*1192A= ENSP00000490415.1:n.*1192A=
ENST00000637244.1:c.*1930A= ENSP00000490188.1:n.*1930A=
ENST00000637343.1:n.2849A=
ENST00000637429.1:c.*1624A= ENSP00000490522.1:n.*1624A=
ENST00000637484.1:c.*1374A= ENSP00000490837.1:n.*1374A=
ENST00000637528.1:c.*224A= ENSP00000490801.1:n.*224A=
ENST00000637609.1:n.4133A=
ENST00000637636.1:c.*224A= ENSP00000490112.1:n.*224A=
ENST00000637752.1:n.1854A=
ENST00000637790.2:c.*224A= MANE Select ENSP00000490272.1:n.*224A=
ENST00000637857.1:n.1778A=
ENST00000637922.1:c.*224A= ENSP00000490071.1:n.*224A=
ENST00000637991.1:c.*224A= ENSP00000489901.1:n.*224A=
ENST00000638028.1:n.1629A=
ENST00000638069.1:n.2233A=
ENST00000262097.10:c.*224A= ENSP00000262097.6:n.*224A=
ENST00000314146.10:c.*224A= ENSP00000326970.10:n.*224A=
ENST00000381733.8:c.*224A= ENSP00000371152.4:n.*224A=
ENST00000520781.5:c.*224A= ENSP00000427751.1:n.*224A=
NM_001127505.1:c.*224A= NP_001120977.1:n.*224A=
NM_001127505.2:c.*224A= NP_001120977.1:n.*224A=
NM_004315.4:c.*224A= NP_004306.3:n.*224A=
NM_004315.5:c.*224A= NP_004306.3:n.*224A=
NM_177924.3:c.*224A= NP_808592.2:n.*224A=
NM_177924.4:c.*224A= NP_808592.2:n.*224A=
XM_005273504.2:c.*224A= XP_005273561.1:n.*224A=
NM_001363743.1:c.*224A= NP_001350672.1:n.*224A=
XM_005273504.3:c.*224A= XP_005273561.1:n.*224A=
NM_177924.5:c.*224A= MANE Select NP_808592.2:n.*224A=
NM_001127505.3:c.*224A= NP_001120977.1:n.*224A=
NM_001363743.2:c.*224A= NP_001350672.1:n.*224A=
NM_004315.6:c.*224A= NP_004306.3:n.*224A=