Canonical Allele Identifier: CA1768025421
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064526T= , CM000670.2:g.18064526T= GRCh38
NC_000008.10:g.17922035T= , CM000670.1:g.17922035T= GRCh37
NC_000008.9:g.17966315T= NCBI36
NG_008985.1:g.25473A=
NG_008985.2:g.25473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.436A= ENSP00000371152.4:p.Ile146=
ENST00000519545.6:n.405A=
ENST00000520781.6:c.383-1296A= ENSP00000427751.1:n.383-1296A=
ENST00000523593.6:c.*231A= ENSP00000490700.1:n.*231A=
ENST00000523744.2:n.4146A=
ENST00000635769.1:c.409A= ENSP00000490485.1:p.Ile137=
ENST00000635944.1:c.*224A= ENSP00000490195.1:n.*224A=
ENST00000635998.1:c.388A= ENSP00000490506.1:p.Ile130=
ENST00000636009.1:c.315-1296A= ENSP00000489988.1:n.315-1296A=
ENST00000636033.1:c.*224A= ENSP00000489617.1:n.*224A=
ENST00000636050.1:c.*231A= ENSP00000490562.1:n.*231A=
ENST00000636128.1:c.382+2694A= ENSP00000489789.1:n.382+2694A=
ENST00000636160.1:c.*280A= ENSP00000489651.1:n.*280A=
ENST00000636171.1:c.383-52A= ENSP00000489761.1:n.383-52A=
ENST00000636299.1:c.*159A= ENSP00000490202.1:n.*159A=
ENST00000636435.1:n.3160A=
ENST00000636455.1:c.436A= ENSP00000490502.1:p.Ile146=
ENST00000636494.1:c.*168A= ENSP00000490388.1:n.*168A=
ENST00000636563.1:n.50A=
ENST00000636577.1:c.383-55A= ENSP00000490027.1:n.383-55A=
ENST00000636691.1:c.193A= ENSP00000490725.1:p.Ile65=
ENST00000636701.1:c.*39A= ENSP00000489800.1:n.*39A=
ENST00000636815.1:c.305A=
ENST00000636823.1:c.193A= ENSP00000490798.1:p.Ile65=
ENST00000636828.1:n.3252A=
ENST00000636920.1:c.*224A= ENSP00000490437.1:n.*224A=
ENST00000636997.1:c.301A= ENSP00000490093.1:p.Ile101=
ENST00000637013.1:c.*600A= ENSP00000490596.1:n.*600A=
ENST00000637095.1:c.*168A= ENSP00000490415.1:n.*168A=
ENST00000637244.1:c.*906A= ENSP00000490188.1:n.*906A=
ENST00000637343.1:n.599A=
ENST00000637429.1:c.*600A= ENSP00000490522.1:n.*600A=
ENST00000637484.1:c.*420-1296A= ENSP00000490837.1:n.*420-1296A=
ENST00000637528.1:c.383-58A= ENSP00000490801.1:n.383-58A=
ENST00000637603.1:c.358A= ENSP00000489979.1:p.Ile120=
ENST00000637609.1:n.3109A=
ENST00000637636.1:c.382A= ENSP00000490112.1:p.Ile128=
ENST00000637638.1:c.388A= ENSP00000490774.1:p.Ile130=
ENST00000637718.1:c.193A= ENSP00000490133.1:p.Ile65=
ENST00000637790.2:c.388A= MANE Select ENSP00000490272.1:p.Ile130=
ENST00000637857.1:n.105-2103A=
ENST00000637922.1:c.193A= ENSP00000490071.1:p.Ile65=
ENST00000637991.1:c.431-1296A= ENSP00000489901.1:n.431-1296A=
ENST00000638069.1:n.444A=
ENST00000262097.10:c.388A= ENSP00000262097.6:p.Ile130=
ENST00000314146.10:c.370A= ENSP00000326970.10:p.Ile124=
ENST00000381733.8:c.436A= ENSP00000371152.4:p.Ile146=
ENST00000519468.5:n.389-2159A=
ENST00000519545.5:n.402A=
ENST00000520781.5:c.383-1296A= ENSP00000427751.1:n.383-1296A=
ENST00000523593.5:n.241A=
ENST00000523744.1:n.391A=
NM_001127505.1:c.370A= NP_001120977.1:p.Ile124=
NM_001127505.2:c.370A= NP_001120977.1:p.Ile124=
NM_004315.4:c.436A= NP_004306.3:p.Ile146=
NM_004315.5:c.436A= NP_004306.3:p.Ile146=
NM_177924.3:c.388A= NP_808592.2:p.Ile130=
NM_177924.4:c.388A= NP_808592.2:p.Ile130=
XM_005273504.2:c.322A= XP_005273561.1:p.Ile108=
NM_001363743.1:c.193A= NP_001350672.1:p.Ile65=
XM_005273504.3:c.322A= XP_005273561.1:p.Ile108=
NM_177924.5:c.388A= MANE Select NP_808592.2:p.Ile130=
NM_001127505.3:c.370A= NP_001120977.1:p.Ile124=
NM_001363743.2:c.193A= NP_001350672.1:p.Ile65=
NM_004315.6:c.436A= NP_004306.3:p.Ile146=