Canonical Allele Identifier: CA1768025402
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064513T= , CM000670.2:g.18064513T= GRCh38
NC_000008.10:g.17922022T= , CM000670.1:g.17922022T= GRCh37
NC_000008.9:g.17966302T= NCBI36
NG_008985.1:g.25486A=
NG_008985.2:g.25486A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.449A= ENSP00000371152.4:p.Asn150=
ENST00000519545.6:n.418A=
ENST00000520781.6:c.383-1283A= ENSP00000427751.1:n.383-1283A=
ENST00000523593.6:c.*244A= ENSP00000490700.1:n.*244A=
ENST00000523744.2:n.4159A=
ENST00000635769.1:c.422A= ENSP00000490485.1:p.Asn141=
ENST00000635944.1:c.*237A= ENSP00000490195.1:n.*237A=
ENST00000635998.1:c.401A= ENSP00000490506.1:p.Asn134=
ENST00000636009.1:c.315-1283A= ENSP00000489988.1:n.315-1283A=
ENST00000636033.1:c.*237A= ENSP00000489617.1:n.*237A=
ENST00000636050.1:c.*244A= ENSP00000490562.1:n.*244A=
ENST00000636128.1:c.382+2707A= ENSP00000489789.1:n.382+2707A=
ENST00000636160.1:c.*293A= ENSP00000489651.1:n.*293A=
ENST00000636171.1:c.383-39A= ENSP00000489761.1:n.383-39A=
ENST00000636299.1:c.*172A= ENSP00000490202.1:n.*172A=
ENST00000636435.1:n.3173A=
ENST00000636455.1:c.449A= ENSP00000490502.1:p.Asn150=
ENST00000636494.1:c.*181A= ENSP00000490388.1:n.*181A=
ENST00000636563.1:n.63A=
ENST00000636577.1:c.383-42A= ENSP00000490027.1:n.383-42A=
ENST00000636691.1:c.206A= ENSP00000490725.1:p.Asn69=
ENST00000636701.1:c.*52A= ENSP00000489800.1:n.*52A=
ENST00000636815.1:c.318A=
ENST00000636823.1:c.206A= ENSP00000490798.1:p.Asn69=
ENST00000636828.1:n.3265A=
ENST00000636920.1:c.*237A= ENSP00000490437.1:n.*237A=
ENST00000636997.1:c.314A= ENSP00000490093.1:p.Asn105=
ENST00000637013.1:c.*613A= ENSP00000490596.1:n.*613A=
ENST00000637095.1:c.*181A= ENSP00000490415.1:n.*181A=
ENST00000637244.1:c.*919A= ENSP00000490188.1:n.*919A=
ENST00000637343.1:n.612A=
ENST00000637429.1:c.*613A= ENSP00000490522.1:n.*613A=
ENST00000637484.1:c.*420-1283A= ENSP00000490837.1:n.*420-1283A=
ENST00000637528.1:c.383-45A= ENSP00000490801.1:n.383-45A=
ENST00000637603.1:c.371A= ENSP00000489979.1:p.Asn124=
ENST00000637609.1:n.3122A=
ENST00000637636.1:c.395A= ENSP00000490112.1:p.Asn132=
ENST00000637638.1:c.401A= ENSP00000490774.1:p.Asn134=
ENST00000637718.1:c.206A= ENSP00000490133.1:p.Asn69=
ENST00000637790.2:c.401A= MANE Select ENSP00000490272.1:p.Asn134=
ENST00000637857.1:n.105-2090A=
ENST00000637922.1:c.206A= ENSP00000490071.1:p.Asn69=
ENST00000637991.1:c.431-1283A= ENSP00000489901.1:n.431-1283A=
ENST00000638069.1:n.457A=
ENST00000262097.10:c.401A= ENSP00000262097.6:p.Asn134=
ENST00000314146.10:c.383A= ENSP00000326970.10:p.Asn128=
ENST00000381733.8:c.449A= ENSP00000371152.4:p.Asn150=
ENST00000519468.5:n.389-2146A=
ENST00000519545.5:n.415A=
ENST00000520781.5:c.383-1283A= ENSP00000427751.1:n.383-1283A=
ENST00000523593.5:n.254A=
ENST00000523744.1:n.404A=
NM_001127505.1:c.383A= NP_001120977.1:p.Asn128=
NM_001127505.2:c.383A= NP_001120977.1:p.Asn128=
NM_004315.4:c.449A= NP_004306.3:p.Asn150=
NM_004315.5:c.449A= NP_004306.3:p.Asn150=
NM_177924.3:c.401A= NP_808592.2:p.Asn134=
NM_177924.4:c.401A= NP_808592.2:p.Asn134=
XM_005273504.2:c.335A= XP_005273561.1:p.Asn112=
NM_001363743.1:c.206A= NP_001350672.1:p.Asn69=
XM_005273504.3:c.335A= XP_005273561.1:p.Asn112=
NM_177924.5:c.401A= MANE Select NP_808592.2:p.Asn134=
NM_001127505.3:c.383A= NP_001120977.1:p.Asn128=
NM_001363743.2:c.206A= NP_001350672.1:p.Asn69=
NM_004315.6:c.449A= NP_004306.3:p.Asn150=