Canonical Allele Identifier: CA2579103701
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451795
ClinVar RCV Id: RCV002007402
dbSNP Id: rs2117037641

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18064530_18064531del , CM000670.2:g.18064530_18064531del GRCh38
NC_000008.10:g.17922039_17922040del , CM000670.1:g.17922039_17922040del GRCh37
NC_000008.9:g.17966319_17966320del NCBI36
NG_008985.1:g.25472_25473del
NG_008985.2:g.25472_25473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.435_436del ENSP00000371152.4:p.Glu145AspfsTer9
ENST00000519545.6:n.404_405del
ENST00000520781.6:c.383-1297_383-1296del ENSP00000427751.1:n.383-1297_383-1296del
ENST00000523593.6:c.*230_*231del ENSP00000490700.1:n.*230_*231del
ENST00000523744.2:n.4145_4146del
ENST00000635769.1:c.408_409del ENSP00000490485.1:p.Glu136AspfsTer9
ENST00000635944.1:c.*223_*224del ENSP00000490195.1:n.*223_*224del
ENST00000635998.1:c.387_388del ENSP00000490506.1:p.Glu129AspfsTer9
ENST00000636009.1:c.315-1297_315-1296del ENSP00000489988.1:n.315-1297_315-1296del
ENST00000636033.1:c.*223_*224del ENSP00000489617.1:n.*223_*224del
ENST00000636050.1:c.*230_*231del ENSP00000490562.1:n.*230_*231del
ENST00000636128.1:c.382+2693_382+2694del ENSP00000489789.1:n.382+2693_382+2694del
ENST00000636160.1:c.*279_*280del ENSP00000489651.1:n.*279_*280del
ENST00000636171.1:c.383-53_383-52del ENSP00000489761.1:n.383-53_383-52del
ENST00000636299.1:c.*158_*159del ENSP00000490202.1:n.*158_*159del
ENST00000636435.1:n.3159_3160del
ENST00000636455.1:c.435_436del ENSP00000490502.1:p.Glu145AspfsTer9
ENST00000636494.1:c.*167_*168del ENSP00000490388.1:n.*167_*168del
ENST00000636563.1:n.49_50del
ENST00000636577.1:c.383-56_383-55del ENSP00000490027.1:n.383-56_383-55del
ENST00000636691.1:c.192_193del ENSP00000490725.1:p.Glu64AspfsTer9
ENST00000636701.1:c.*38_*39del ENSP00000489800.1:n.*38_*39del
ENST00000636815.1:c.304_305del
ENST00000636823.1:c.192_193del ENSP00000490798.1:p.Glu64AspfsTer9
ENST00000636828.1:n.3251_3252del
ENST00000636920.1:c.*223_*224del ENSP00000490437.1:n.*223_*224del
ENST00000636997.1:c.300_301del ENSP00000490093.1:p.Glu100AspfsTer9
ENST00000637013.1:c.*599_*600del ENSP00000490596.1:n.*599_*600del
ENST00000637095.1:c.*167_*168del ENSP00000490415.1:n.*167_*168del
ENST00000637244.1:c.*905_*906del ENSP00000490188.1:n.*905_*906del
ENST00000637343.1:n.598_599del
ENST00000637429.1:c.*599_*600del ENSP00000490522.1:n.*599_*600del
ENST00000637484.1:c.*420-1297_*420-1296del ENSP00000490837.1:n.*420-1297_*420-1296del
ENST00000637528.1:c.383-59_383-58del ENSP00000490801.1:n.383-59_383-58del
ENST00000637603.1:c.357_358del ENSP00000489979.1:p.Glu119AspfsTer9
ENST00000637609.1:n.3108_3109del
ENST00000637636.1:c.381_382del ENSP00000490112.1:p.Glu127AspfsTer9
ENST00000637638.1:c.387_388del ENSP00000490774.1:p.Glu129AspfsTer9
ENST00000637718.1:c.192_193del ENSP00000490133.1:p.Glu64AspfsTer9
ENST00000637790.2:c.387_388del MANE Select ENSP00000490272.1:p.Glu129AspfsTer9
ENST00000637857.1:n.105-2104_105-2103del
ENST00000637922.1:c.192_193del ENSP00000490071.1:p.Glu64AspfsTer9
ENST00000637991.1:c.431-1297_431-1296del ENSP00000489901.1:n.431-1297_431-1296del
ENST00000638069.1:n.443_444del
ENST00000262097.10:c.387_388del ENSP00000262097.6:p.Glu129AspfsTer9
ENST00000314146.10:c.369_370del ENSP00000326970.10:p.Glu123AspfsTer9
ENST00000381733.8:c.435_436del ENSP00000371152.4:p.Glu145AspfsTer9
ENST00000519468.5:n.389-2160_389-2159del
ENST00000519545.5:n.401_402del
ENST00000520781.5:c.383-1297_383-1296del ENSP00000427751.1:n.383-1297_383-1296del
ENST00000523593.5:n.240_241del
ENST00000523744.1:n.390_391del
NM_001127505.1:c.369_370del NP_001120977.1:p.Glu123AspfsTer9
NM_001127505.2:c.369_370del NP_001120977.1:p.Glu123AspfsTer9
NM_004315.4:c.435_436del NP_004306.3:p.Glu145AspfsTer9
NM_004315.5:c.435_436del NP_004306.3:p.Glu145AspfsTer9
NM_177924.3:c.387_388del NP_808592.2:p.Glu129AspfsTer9
NM_177924.4:c.387_388del NP_808592.2:p.Glu129AspfsTer9
XM_005273504.2:c.321_322del XP_005273561.1:p.Glu107AspfsTer9
NM_001363743.1:c.192_193del NP_001350672.1:p.Glu64AspfsTer9
XM_005273504.3:c.321_322del XP_005273561.1:p.Glu107AspfsTer9
NM_177924.5:c.387_388del MANE Select NP_808592.2:p.Glu129AspfsTer9
NM_001127505.3:c.369_370del NP_001120977.1:p.Glu123AspfsTer9
NM_001363743.2:c.192_193del NP_001350672.1:p.Glu64AspfsTer9
NM_004315.6:c.435_436del NP_004306.3:p.Glu145AspfsTer9