Canonical Allele Identifier: CA375227486

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133346883G>T (hg19) ; chr9:g.130471496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130471496G>T , CM000671.2:g.130471496G>T	GRCh38
NC_000009.11:g.133346883G>T , CM000671.1:g.133346883G>T	GRCh37
NC_000009.10:g.132336704G>T	NCBI36
NG_011542.1:g.31790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.578G>T MANE Select	ENSP00000253004.6:p.Gly193Val
ENST00000352480.9:c.578G>T	ENSP00000253004.6:p.Gly193Val
ENST00000372393.7:c.578G>T	ENSP00000361469.2:p.Gly193Val
ENST00000372394.5:c.578G>T	ENSP00000361471.1:p.Gly193Val
ENST00000422569.5:c.578G>T	ENSP00000394212.1:p.Gly193Val
ENST00000443588.1:c.521G>T	ENSP00000397785.1:p.Gly174Val
ENST00000467695.5:n.287G>T
ENST00000493984.6:n.409G>T
NM_000050.4:c.578G>T	NP_000041.2:p.Gly193Val
NM_054012.3:c.578G>T	NP_446464.1:p.Gly193Val
XM_005272200.2:c.578G>T	XP_005272257.1:p.Gly193Val
XM_011518705.1:c.692G>T	XP_011517007.1:p.Gly231Val
XM_005272200.3:c.578G>T	XP_005272257.1:p.Gly193Val
XM_011518705.2:c.692G>T	XP_011517007.1:p.Gly231Val
XM_017014729.1:c.674G>T	XP_016870218.1:p.Gly225Val
NM_054012.4:c.578G>T MANE Select	NP_446464.1:p.Gly193Val