Canonical Allele Identifier: CA370431761

Gene: ASAH1

Linked Data

• MyVariant Identifiers: chr8:g.17922020T>G (hg19) ; chr8:g.18064511T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18064511T>G , CM000670.2:g.18064511T>G	GRCh38
NC_000008.10:g.17922020T>G , CM000670.1:g.17922020T>G	GRCh37
NC_000008.9:g.17966300T>G	NCBI36
NG_008985.1:g.25488A>C
NG_008985.2:g.25488A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.451A>C	ENSP00000371152.4:p.Ile151Leu
ENST00000519545.6:n.420A>C
ENST00000520781.6:c.383-1281A>C	ENSP00000427751.1:n.383-1281A>C
ENST00000523593.6:c.*246A>C	ENSP00000490700.1:n.*246A>C
ENST00000523744.2:n.4161A>C
ENST00000635769.1:c.424A>C	ENSP00000490485.1:p.Ile142Leu
ENST00000635944.1:c.*239A>C	ENSP00000490195.1:n.*239A>C
ENST00000635998.1:c.403A>C	ENSP00000490506.1:p.Ile135Leu
ENST00000636009.1:c.315-1281A>C	ENSP00000489988.1:n.315-1281A>C
ENST00000636033.1:c.*239A>C	ENSP00000489617.1:n.*239A>C
ENST00000636050.1:c.*246A>C	ENSP00000490562.1:n.*246A>C
ENST00000636128.1:c.382+2709A>C	ENSP00000489789.1:n.382+2709A>C
ENST00000636160.1:c.*295A>C	ENSP00000489651.1:n.*295A>C
ENST00000636171.1:c.383-37A>C	ENSP00000489761.1:n.383-37A>C
ENST00000636299.1:c.*174A>C	ENSP00000490202.1:n.*174A>C
ENST00000636435.1:n.3175A>C
ENST00000636455.1:c.451A>C	ENSP00000490502.1:p.Ile151Leu
ENST00000636494.1:c.*183A>C	ENSP00000490388.1:n.*183A>C
ENST00000636563.1:n.65A>C
ENST00000636577.1:c.383-40A>C	ENSP00000490027.1:n.383-40A>C
ENST00000636691.1:c.208A>C	ENSP00000490725.1:p.Ile70Leu
ENST00000636701.1:c.*54A>C	ENSP00000489800.1:n.*54A>C
ENST00000636815.1:c.320A>C
ENST00000636823.1:c.208A>C	ENSP00000490798.1:p.Ile70Leu
ENST00000636828.1:n.3267A>C
ENST00000636920.1:c.*239A>C	ENSP00000490437.1:n.*239A>C
ENST00000636997.1:c.316A>C	ENSP00000490093.1:p.Ile106Leu
ENST00000637013.1:c.*615A>C	ENSP00000490596.1:n.*615A>C
ENST00000637095.1:c.*183A>C	ENSP00000490415.1:n.*183A>C
ENST00000637244.1:c.*921A>C	ENSP00000490188.1:n.*921A>C
ENST00000637343.1:n.614A>C
ENST00000637429.1:c.*615A>C	ENSP00000490522.1:n.*615A>C
ENST00000637484.1:c.*420-1281A>C	ENSP00000490837.1:n.*420-1281A>C
ENST00000637528.1:c.383-43A>C	ENSP00000490801.1:n.383-43A>C
ENST00000637603.1:c.373A>C	ENSP00000489979.1:p.Ile125Leu
ENST00000637609.1:n.3124A>C
ENST00000637636.1:c.397A>C	ENSP00000490112.1:p.Ile133Leu
ENST00000637638.1:c.403A>C	ENSP00000490774.1:p.Ile135Leu
ENST00000637718.1:c.208A>C	ENSP00000490133.1:p.Ile70Leu
ENST00000637790.2:c.403A>C MANE Select	ENSP00000490272.1:p.Ile135Leu
ENST00000637857.1:n.105-2088A>C
ENST00000637922.1:c.208A>C	ENSP00000490071.1:p.Ile70Leu
ENST00000637991.1:c.431-1281A>C	ENSP00000489901.1:n.431-1281A>C
ENST00000638069.1:n.459A>C
ENST00000262097.10:c.403A>C	ENSP00000262097.6:p.Ile135Leu
ENST00000314146.10:c.385A>C	ENSP00000326970.10:p.Ile129Leu
ENST00000381733.8:c.451A>C	ENSP00000371152.4:p.Ile151Leu
ENST00000519468.5:n.389-2144A>C
ENST00000519545.5:n.417A>C
ENST00000520781.5:c.383-1281A>C	ENSP00000427751.1:n.383-1281A>C
ENST00000523593.5:n.256A>C
ENST00000523744.1:n.406A>C
NM_001127505.1:c.385A>C	NP_001120977.1:p.Ile129Leu
NM_001127505.2:c.385A>C	NP_001120977.1:p.Ile129Leu
NM_004315.4:c.451A>C	NP_004306.3:p.Ile151Leu
NM_004315.5:c.451A>C	NP_004306.3:p.Ile151Leu
NM_177924.3:c.403A>C	NP_808592.2:p.Ile135Leu
NM_177924.4:c.403A>C	NP_808592.2:p.Ile135Leu
XM_005273504.2:c.337A>C	XP_005273561.1:p.Ile113Leu
NM_001363743.1:c.208A>C	NP_001350672.1:p.Ile70Leu
XM_005273504.3:c.337A>C	XP_005273561.1:p.Ile113Leu
NM_177924.5:c.403A>C MANE Select	NP_808592.2:p.Ile135Leu
NM_001127505.3:c.385A>C	NP_001120977.1:p.Ile129Leu
NM_001363743.2:c.208A>C	NP_001350672.1:p.Ile70Leu
NM_004315.6:c.451A>C	NP_004306.3:p.Ile151Leu