Canonical Allele Identifier: CA375223495

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133327637G>A (hg19) ; chr9:g.130452250G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452250G>A , CM000671.2:g.130452250G>A	GRCh38
NC_000009.11:g.133327637G>A , CM000671.1:g.133327637G>A	GRCh37
NC_000009.10:g.132317458G>A	NCBI36
NG_011542.1:g.12544G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.22G>A MANE Select	ENSP00000253004.6:p.Val8Ile
ENST00000352480.9:c.22G>A	ENSP00000253004.6:p.Val8Ile
ENST00000372393.7:c.22G>A	ENSP00000361469.2:p.Val8Ile
ENST00000372394.5:c.22G>A	ENSP00000361471.1:p.Val8Ile
ENST00000422569.5:c.22G>A	ENSP00000394212.1:p.Val8Ile
ENST00000443588.1:c.22G>A	ENSP00000397785.1:p.Val8Ile
NM_000050.4:c.22G>A	NP_000041.2:p.Val8Ile
NM_054012.3:c.22G>A	NP_446464.1:p.Val8Ile
XM_005272200.2:c.22G>A	XP_005272257.1:p.Val8Ile
XM_011518705.1:c.136G>A	XP_011517007.1:p.Val46Ile
XM_005272200.3:c.22G>A	XP_005272257.1:p.Val8Ile
XM_011518705.2:c.136G>A	XP_011517007.1:p.Val46Ile
XM_017014729.1:c.118G>A	XP_016870218.1:p.Val40Ile
NM_054012.4:c.22G>A MANE Select	NP_446464.1:p.Val8Ile