Canonical Allele Identifier: CA1768025354
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064497T= , CM000670.2:g.18064497T= GRCh38
NC_000008.10:g.17922006T= , CM000670.1:g.17922006T= GRCh37
NC_000008.9:g.17966286T= NCBI36
NG_008985.1:g.25502A=
NG_008985.2:g.25502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.465A= ENSP00000371152.4:p.Leu155=
ENST00000519545.6:n.434A=
ENST00000520781.6:c.383-1267A= ENSP00000427751.1:n.383-1267A=
ENST00000523593.6:c.*260A= ENSP00000490700.1:n.*260A=
ENST00000523744.2:n.4175A=
ENST00000635769.1:c.438A= ENSP00000490485.1:p.Leu146=
ENST00000635944.1:c.*253A= ENSP00000490195.1:n.*253A=
ENST00000635998.1:c.417A= ENSP00000490506.1:p.Leu139=
ENST00000636009.1:c.315-1267A= ENSP00000489988.1:n.315-1267A=
ENST00000636033.1:c.*253A= ENSP00000489617.1:n.*253A=
ENST00000636050.1:c.*260A= ENSP00000490562.1:n.*260A=
ENST00000636128.1:c.382+2723A= ENSP00000489789.1:n.382+2723A=
ENST00000636160.1:c.*309A= ENSP00000489651.1:n.*309A=
ENST00000636171.1:c.383-23A= ENSP00000489761.1:n.383-23A=
ENST00000636299.1:c.*188A= ENSP00000490202.1:n.*188A=
ENST00000636435.1:n.3189A=
ENST00000636455.1:c.465A= ENSP00000490502.1:p.Leu155=
ENST00000636494.1:c.*197A= ENSP00000490388.1:n.*197A=
ENST00000636563.1:n.79A=
ENST00000636577.1:c.383-26A= ENSP00000490027.1:n.383-26A=
ENST00000636691.1:c.222A= ENSP00000490725.1:p.Leu74=
ENST00000636701.1:c.*68A= ENSP00000489800.1:n.*68A=
ENST00000636815.1:c.334A=
ENST00000636823.1:c.222A= ENSP00000490798.1:p.Leu74=
ENST00000636828.1:n.3281A=
ENST00000636920.1:c.*253A= ENSP00000490437.1:n.*253A=
ENST00000636997.1:c.330A= ENSP00000490093.1:p.Leu110=
ENST00000637013.1:c.*629A= ENSP00000490596.1:n.*629A=
ENST00000637095.1:c.*197A= ENSP00000490415.1:n.*197A=
ENST00000637244.1:c.*935A= ENSP00000490188.1:n.*935A=
ENST00000637343.1:n.628A=
ENST00000637429.1:c.*629A= ENSP00000490522.1:n.*629A=
ENST00000637484.1:c.*420-1267A= ENSP00000490837.1:n.*420-1267A=
ENST00000637528.1:c.383-29A= ENSP00000490801.1:n.383-29A=
ENST00000637603.1:c.387A= ENSP00000489979.1:p.Leu129=
ENST00000637609.1:n.3138A=
ENST00000637636.1:c.411A= ENSP00000490112.1:p.Leu137=
ENST00000637638.1:c.417A= ENSP00000490774.1:p.Leu139=
ENST00000637718.1:c.222A= ENSP00000490133.1:p.Leu74=
ENST00000637790.2:c.417A= MANE Select ENSP00000490272.1:p.Leu139=
ENST00000637857.1:n.105-2074A=
ENST00000637922.1:c.222A= ENSP00000490071.1:p.Leu74=
ENST00000637991.1:c.431-1267A= ENSP00000489901.1:n.431-1267A=
ENST00000638069.1:n.473A=
ENST00000262097.10:c.417A= ENSP00000262097.6:p.Leu139=
ENST00000314146.10:c.399A= ENSP00000326970.10:p.Leu133=
ENST00000381733.8:c.465A= ENSP00000371152.4:p.Leu155=
ENST00000519468.5:n.389-2130A=
ENST00000519545.5:n.431A=
ENST00000520781.5:c.383-1267A= ENSP00000427751.1:n.383-1267A=
ENST00000523593.5:n.270A=
ENST00000523744.1:n.420A=
NM_001127505.1:c.399A= NP_001120977.1:p.Leu133=
NM_001127505.2:c.399A= NP_001120977.1:p.Leu133=
NM_004315.4:c.465A= NP_004306.3:p.Leu155=
NM_004315.5:c.465A= NP_004306.3:p.Leu155=
NM_177924.3:c.417A= NP_808592.2:p.Leu139=
NM_177924.4:c.417A= NP_808592.2:p.Leu139=
XM_005273504.2:c.351A= XP_005273561.1:p.Leu117=
NM_001363743.1:c.222A= NP_001350672.1:p.Leu74=
XM_005273504.3:c.351A= XP_005273561.1:p.Leu117=
NM_177924.5:c.417A= MANE Select NP_808592.2:p.Leu139=
NM_001127505.3:c.399A= NP_001120977.1:p.Leu133=
NM_001363743.2:c.222A= NP_001350672.1:p.Leu74=
NM_004315.6:c.465A= NP_004306.3:p.Leu155=