Canonical Allele Identifier: CA370431735

Gene: ASAH1

Linked Data

• MyVariant Identifiers: chr8:g.17922016A>G (hg19) ; chr8:g.18064507A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18064507A>G , CM000670.2:g.18064507A>G	GRCh38
NC_000008.10:g.17922016A>G , CM000670.1:g.17922016A>G	GRCh37
NC_000008.9:g.17966296A>G	NCBI36
NG_008985.1:g.25492T>C
NG_008985.2:g.25492T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381733.9:c.455T>C	ENSP00000371152.4:p.Phe152Ser
ENST00000519545.6:n.424T>C
ENST00000520781.6:c.383-1277T>C	ENSP00000427751.1:n.383-1277T>C
ENST00000523593.6:c.*250T>C	ENSP00000490700.1:n.*250T>C
ENST00000523744.2:n.4165T>C
ENST00000635769.1:c.428T>C	ENSP00000490485.1:p.Phe143Ser
ENST00000635944.1:c.*243T>C	ENSP00000490195.1:n.*243T>C
ENST00000635998.1:c.407T>C	ENSP00000490506.1:p.Phe136Ser
ENST00000636009.1:c.315-1277T>C	ENSP00000489988.1:n.315-1277T>C
ENST00000636033.1:c.*243T>C	ENSP00000489617.1:n.*243T>C
ENST00000636050.1:c.*250T>C	ENSP00000490562.1:n.*250T>C
ENST00000636128.1:c.382+2713T>C	ENSP00000489789.1:n.382+2713T>C
ENST00000636160.1:c.*299T>C	ENSP00000489651.1:n.*299T>C
ENST00000636171.1:c.383-33T>C	ENSP00000489761.1:n.383-33T>C
ENST00000636299.1:c.*178T>C	ENSP00000490202.1:n.*178T>C
ENST00000636435.1:n.3179T>C
ENST00000636455.1:c.455T>C	ENSP00000490502.1:p.Phe152Ser
ENST00000636494.1:c.*187T>C	ENSP00000490388.1:n.*187T>C
ENST00000636563.1:n.69T>C
ENST00000636577.1:c.383-36T>C	ENSP00000490027.1:n.383-36T>C
ENST00000636691.1:c.212T>C	ENSP00000490725.1:p.Phe71Ser
ENST00000636701.1:c.*58T>C	ENSP00000489800.1:n.*58T>C
ENST00000636815.1:c.324T>C
ENST00000636823.1:c.212T>C	ENSP00000490798.1:p.Phe71Ser
ENST00000636828.1:n.3271T>C
ENST00000636920.1:c.*243T>C	ENSP00000490437.1:n.*243T>C
ENST00000636997.1:c.320T>C	ENSP00000490093.1:p.Phe107Ser
ENST00000637013.1:c.*619T>C	ENSP00000490596.1:n.*619T>C
ENST00000637095.1:c.*187T>C	ENSP00000490415.1:n.*187T>C
ENST00000637244.1:c.*925T>C	ENSP00000490188.1:n.*925T>C
ENST00000637343.1:n.618T>C
ENST00000637429.1:c.*619T>C	ENSP00000490522.1:n.*619T>C
ENST00000637484.1:c.*420-1277T>C	ENSP00000490837.1:n.*420-1277T>C
ENST00000637528.1:c.383-39T>C	ENSP00000490801.1:n.383-39T>C
ENST00000637603.1:c.377T>C	ENSP00000489979.1:p.Phe126Ser
ENST00000637609.1:n.3128T>C
ENST00000637636.1:c.401T>C	ENSP00000490112.1:p.Phe134Ser
ENST00000637638.1:c.407T>C	ENSP00000490774.1:p.Phe136Ser
ENST00000637718.1:c.212T>C	ENSP00000490133.1:p.Phe71Ser
ENST00000637790.2:c.407T>C MANE Select	ENSP00000490272.1:p.Phe136Ser
ENST00000637857.1:n.105-2084T>C
ENST00000637922.1:c.212T>C	ENSP00000490071.1:p.Phe71Ser
ENST00000637991.1:c.431-1277T>C	ENSP00000489901.1:n.431-1277T>C
ENST00000638069.1:n.463T>C
ENST00000262097.10:c.407T>C	ENSP00000262097.6:p.Phe136Ser
ENST00000314146.10:c.389T>C	ENSP00000326970.10:p.Phe130Ser
ENST00000381733.8:c.455T>C	ENSP00000371152.4:p.Phe152Ser
ENST00000519468.5:n.389-2140T>C
ENST00000519545.5:n.421T>C
ENST00000520781.5:c.383-1277T>C	ENSP00000427751.1:n.383-1277T>C
ENST00000523593.5:n.260T>C
ENST00000523744.1:n.410T>C
NM_001127505.1:c.389T>C	NP_001120977.1:p.Phe130Ser
NM_001127505.2:c.389T>C	NP_001120977.1:p.Phe130Ser
NM_004315.4:c.455T>C	NP_004306.3:p.Phe152Ser
NM_004315.5:c.455T>C	NP_004306.3:p.Phe152Ser
NM_177924.3:c.407T>C	NP_808592.2:p.Phe136Ser
NM_177924.4:c.407T>C	NP_808592.2:p.Phe136Ser
XM_005273504.2:c.341T>C	XP_005273561.1:p.Phe114Ser
NM_001363743.1:c.212T>C	NP_001350672.1:p.Phe71Ser
XM_005273504.3:c.341T>C	XP_005273561.1:p.Phe114Ser
NM_177924.5:c.407T>C MANE Select	NP_808592.2:p.Phe136Ser
NM_001127505.3:c.389T>C	NP_001120977.1:p.Phe130Ser
NM_001363743.2:c.212T>C	NP_001350672.1:p.Phe71Ser
NM_004315.6:c.455T>C	NP_004306.3:p.Phe152Ser