Canonical Allele Identifier: CA370429426

Gene: ASAH1

Linked Data

• MyVariant Identifiers: chr8:g.17918941T>A (hg19) ; chr8:g.18061432T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061432T>A , CM000670.2:g.18061432T>A	GRCh38
NC_000008.10:g.17918941T>A , CM000670.1:g.17918941T>A	GRCh37
NC_000008.9:g.17963221T>A	NCBI36
NG_008985.1:g.28567A>T
NG_008985.2:g.28567A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381733.9:c.778A>T	ENSP00000371152.4:p.Lys260Ter
ENST00000517409.2:n.698A>T
ENST00000518746.2:n.2416A>T
ENST00000519545.6:n.747A>T
ENST00000520781.6:c.655A>T	ENSP00000427751.1:p.Lys219Ter
ENST00000521542.2:n.38A>T
ENST00000635756.1:c.143A>T
ENST00000635944.1:c.*566A>T	ENSP00000490195.1:n.*566A>T
ENST00000635998.1:c.730A>T	ENSP00000490506.1:p.Lys244Ter
ENST00000636009.1:c.587A>T	ENSP00000489988.1:n.587A>T
ENST00000636033.1:c.*566A>T	ENSP00000489617.1:n.*566A>T
ENST00000636050.1:c.*573A>T	ENSP00000490562.1:n.*573A>T
ENST00000636128.1:c.409A>T	ENSP00000489789.1:p.Lys137Ter
ENST00000636160.1:c.*622A>T	ENSP00000489651.1:n.*622A>T
ENST00000636171.1:c.673A>T	ENSP00000489761.1:p.Lys225Ter
ENST00000636455.1:c.778A>T	ENSP00000490502.1:p.Lys260Ter
ENST00000636494.1:c.*510A>T	ENSP00000490388.1:n.*510A>T
ENST00000636563.1:n.392A>T
ENST00000636577.1:c.670A>T	ENSP00000490027.1:p.Lys224Ter
ENST00000636691.1:c.535A>T	ENSP00000490725.1:p.Lys179Ter
ENST00000636701.1:c.*381A>T	ENSP00000489800.1:n.*381A>T
ENST00000636815.1:c.647A>T
ENST00000636920.1:c.*566A>T	ENSP00000490437.1:n.*566A>T
ENST00000636997.1:c.643A>T	ENSP00000490093.1:p.Lys215Ter
ENST00000637013.1:c.*1098A>T	ENSP00000490596.1:n.*1098A>T
ENST00000637014.1:n.1137A>T
ENST00000637095.1:c.*510A>T	ENSP00000490415.1:n.*510A>T
ENST00000637244.1:c.*1248A>T	ENSP00000490188.1:n.*1248A>T
ENST00000637343.1:n.2167A>T
ENST00000637429.1:c.*942A>T	ENSP00000490522.1:n.*942A>T
ENST00000637484.1:c.*692A>T	ENSP00000490837.1:n.*692A>T
ENST00000637528.1:c.667A>T	ENSP00000490801.1:p.Lys223Ter
ENST00000637609.1:n.3451A>T
ENST00000637636.1:c.724A>T	ENSP00000490112.1:p.Lys242Ter
ENST00000637790.2:c.730A>T MANE Select	ENSP00000490272.1:p.Lys244Ter
ENST00000637857.1:n.1096A>T
ENST00000637922.1:c.535A>T	ENSP00000490071.1:p.Lys179Ter
ENST00000637991.1:c.703A>T	ENSP00000489901.1:p.Lys235Ter
ENST00000638028.1:n.947A>T
ENST00000638069.1:n.1551A>T
ENST00000262097.10:c.730A>T	ENSP00000262097.6:p.Lys244Ter
ENST00000314146.10:c.712A>T	ENSP00000326970.10:p.Lys238Ter
ENST00000381733.8:c.778A>T	ENSP00000371152.4:p.Lys260Ter
ENST00000518746.1:n.547A>T
ENST00000519468.5:n.559A>T
ENST00000520781.5:c.655A>T	ENSP00000427751.1:p.Lys219Ter
ENST00000521542.1:n.443A>T
NM_001127505.1:c.712A>T	NP_001120977.1:p.Lys238Ter
NM_001127505.2:c.712A>T	NP_001120977.1:p.Lys238Ter
NM_004315.4:c.778A>T	NP_004306.3:p.Lys260Ter
NM_004315.5:c.778A>T	NP_004306.3:p.Lys260Ter
NM_177924.3:c.730A>T	NP_808592.2:p.Lys244Ter
NM_177924.4:c.730A>T	NP_808592.2:p.Lys244Ter
XM_005273504.2:c.664A>T	XP_005273561.1:p.Lys222Ter
NM_001363743.1:c.535A>T	NP_001350672.1:p.Lys179Ter
XM_005273504.3:c.664A>T	XP_005273561.1:p.Lys222Ter
NM_177924.5:c.730A>T MANE Select	NP_808592.2:p.Lys244Ter
NM_001127505.3:c.712A>T	NP_001120977.1:p.Lys238Ter
NM_001363743.2:c.535A>T	NP_001350672.1:p.Lys179Ter
NM_004315.6:c.778A>T	NP_004306.3:p.Lys260Ter