Canonical Allele Identifier: CA1111404263
Gene: ASAH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064927_18064930del , CM000670.2:g.18064927_18064930del GRCh38
NC_000008.10:g.17922436_17922439del , CM000670.1:g.17922436_17922439del GRCh37
NC_000008.9:g.17966716_17966719del NCBI36
NG_008985.1:g.25069_25072del
NG_008985.2:g.25069_25072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.431-399_431-396del ENSP00000371152.4:n.431-399_431-396del
ENST00000519545.6:n.400-399_400-396del
ENST00000520781.6:c.383-1700_383-1697del ENSP00000427751.1:n.383-1700_383-1697del
ENST00000523593.6:c.*226-399_*226-396del ENSP00000490700.1:n.*226-399_*226-396del
ENST00000523744.2:n.3742_3745del
ENST00000635769.1:c.404-399_404-396del ENSP00000490485.1:n.404-399_404-396del
ENST00000635944.1:c.*219-399_*219-396del ENSP00000490195.1:n.*219-399_*219-396del
ENST00000635998.1:c.383-399_383-396del ENSP00000490506.1:n.383-399_383-396del
ENST00000636009.1:c.315-1700_315-1697del ENSP00000489988.1:n.315-1700_315-1697del
ENST00000636033.1:c.*219-399_*219-396del ENSP00000489617.1:n.*219-399_*219-396del
ENST00000636050.1:c.*226-399_*226-396del ENSP00000490562.1:n.*226-399_*226-396del
ENST00000636128.1:c.382+2290_382+2293del ENSP00000489789.1:n.382+2290_382+2293del
ENST00000636160.1:c.*275-399_*275-396del ENSP00000489651.1:n.*275-399_*275-396del
ENST00000636171.1:c.383-456_383-453del ENSP00000489761.1:n.383-456_383-453del
ENST00000636299.1:c.*154-399_*154-396del ENSP00000490202.1:n.*154-399_*154-396del
ENST00000636435.1:n.2756_2759del
ENST00000636455.1:c.431-399_431-396del ENSP00000490502.1:n.431-399_431-396del
ENST00000636494.1:c.*163-399_*163-396del ENSP00000490388.1:n.*163-399_*163-396del
ENST00000636577.1:c.383-459_383-456del ENSP00000490027.1:n.383-459_383-456del
ENST00000636691.1:c.188-399_188-396del ENSP00000490725.1:n.188-399_188-396del
ENST00000636701.1:c.*34-399_*34-396del ENSP00000489800.1:n.*34-399_*34-396del
ENST00000636815.1:c.300-399_300-396del
ENST00000636823.1:c.188-399_188-396del ENSP00000490798.1:n.188-399_188-396del
ENST00000636828.1:n.2848_2851del
ENST00000636920.1:c.*219-399_*219-396del ENSP00000490437.1:n.*219-399_*219-396del
ENST00000636997.1:c.296-399_296-396del ENSP00000490093.1:n.296-399_296-396del
ENST00000637013.1:c.*595-399_*595-396del ENSP00000490596.1:n.*595-399_*595-396del
ENST00000637095.1:c.*163-399_*163-396del ENSP00000490415.1:n.*163-399_*163-396del
ENST00000637244.1:c.*901-399_*901-396del ENSP00000490188.1:n.*901-399_*901-396del
ENST00000637343.1:n.195_198del
ENST00000637429.1:c.*595-399_*595-396del ENSP00000490522.1:n.*595-399_*595-396del
ENST00000637484.1:c.*420-1700_*420-1697del ENSP00000490837.1:n.*420-1700_*420-1697del
ENST00000637528.1:c.383-462_383-459del ENSP00000490801.1:n.383-462_383-459del
ENST00000637603.1:c.353-399_353-396del ENSP00000489979.1:n.353-399_353-396del
ENST00000637609.1:n.2705_2708del
ENST00000637636.1:c.377-399_377-396del ENSP00000490112.1:n.377-399_377-396del
ENST00000637638.1:c.383-399_383-396del ENSP00000490774.1:n.383-399_383-396del
ENST00000637718.1:c.188-399_188-396del ENSP00000490133.1:n.188-399_188-396del
ENST00000637790.2:c.383-399_383-396del MANE Select ENSP00000490272.1:n.383-399_383-396del
ENST00000637857.1:n.104+2290_104+2293del
ENST00000637922.1:c.188-399_188-396del ENSP00000490071.1:n.188-399_188-396del
ENST00000637991.1:c.431-1700_431-1697del ENSP00000489901.1:n.431-1700_431-1697del
ENST00000638069.1:n.439-399_439-396del
ENST00000262097.10:c.383-399_383-396del ENSP00000262097.6:n.383-399_383-396del
ENST00000314146.10:c.365-399_365-396del ENSP00000326970.10:n.365-399_365-396del
ENST00000381733.8:c.431-399_431-396del ENSP00000371152.4:n.431-399_431-396del
ENST00000519468.5:n.388+2290_388+2293del
ENST00000519545.5:n.397-399_397-396del
ENST00000520781.5:c.383-1700_383-1697del ENSP00000427751.1:n.383-1700_383-1697del
ENST00000523593.5:n.236-399_236-396del
NM_001127505.1:c.365-399_365-396del NP_001120977.1:n.365-399_365-396del
NM_001127505.2:c.365-399_365-396del NP_001120977.1:n.365-399_365-396del
NM_004315.4:c.431-399_431-396del NP_004306.3:n.431-399_431-396del
NM_004315.5:c.431-399_431-396del NP_004306.3:n.431-399_431-396del
NM_177924.3:c.383-399_383-396del NP_808592.2:n.383-399_383-396del
NM_177924.4:c.383-399_383-396del NP_808592.2:n.383-399_383-396del
XM_005273504.2:c.317-399_317-396del XP_005273561.1:n.317-399_317-396del
NM_001363743.1:c.188-399_188-396del NP_001350672.1:n.188-399_188-396del
XM_005273504.3:c.317-399_317-396del XP_005273561.1:n.317-399_317-396del
NM_177924.5:c.383-399_383-396del MANE Select NP_808592.2:n.383-399_383-396del
NM_001127505.3:c.365-399_365-396del NP_001120977.1:n.365-399_365-396del
NM_001363743.2:c.188-399_188-396del NP_001350672.1:n.188-399_188-396del
NM_004315.6:c.431-399_431-396del NP_004306.3:n.431-399_431-396del