Canonical Allele Identifier: CA375227520

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133346892A>T (hg19) ; chr9:g.130471505A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130471505A>T , CM000671.2:g.130471505A>T	GRCh38
NC_000009.11:g.133346892A>T , CM000671.1:g.133346892A>T	GRCh37
NC_000009.10:g.132336713A>T	NCBI36
NG_011542.1:g.31799A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.587A>T MANE Select	ENSP00000253004.6:p.Glu196Val
ENST00000352480.9:c.587A>T	ENSP00000253004.6:p.Glu196Val
ENST00000372393.7:c.587A>T	ENSP00000361469.2:p.Glu196Val
ENST00000372394.5:c.587A>T	ENSP00000361471.1:p.Glu196Val
ENST00000422569.5:c.587A>T	ENSP00000394212.1:p.Glu196Val
ENST00000443588.1:c.530A>T	ENSP00000397785.1:p.Glu177Val
ENST00000467695.5:n.296A>T
ENST00000493984.6:n.418A>T
NM_000050.4:c.587A>T	NP_000041.2:p.Glu196Val
NM_054012.3:c.587A>T	NP_446464.1:p.Glu196Val
XM_005272200.2:c.587A>T	XP_005272257.1:p.Glu196Val
XM_011518705.1:c.701A>T	XP_011517007.1:p.Glu234Val
XM_005272200.3:c.587A>T	XP_005272257.1:p.Glu196Val
XM_011518705.2:c.701A>T	XP_011517007.1:p.Glu234Val
XM_017014729.1:c.683A>T	XP_016870218.1:p.Glu228Val
NM_054012.4:c.587A>T MANE Select	NP_446464.1:p.Glu196Val