Canonical Allele Identifier: CA375230634

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364798T>A (hg19) ; chr9:g.130489411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489411T>A , CM000671.2:g.130489411T>A	GRCh38
NC_000009.11:g.133364798T>A , CM000671.1:g.133364798T>A	GRCh37
NC_000009.10:g.132354619T>A	NCBI36
NG_011542.1:g.49705T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.917T>A MANE Select	ENSP00000253004.6:p.Val306Glu
ENST00000352480.9:c.917T>A	ENSP00000253004.6:p.Val306Glu
ENST00000372386.6:n.188T>A
ENST00000372393.7:c.917T>A	ENSP00000361469.2:p.Val306Glu
ENST00000372394.5:c.917T>A	ENSP00000361471.1:p.Val306Glu
ENST00000470849.4:n.642T>A
ENST00000492400.5:n.426T>A
NM_000050.4:c.917T>A	NP_000041.2:p.Val306Glu
NM_054012.3:c.917T>A	NP_446464.1:p.Val306Glu
XM_005272200.2:c.917T>A	XP_005272257.1:p.Val306Glu
XM_011518705.1:c.1031T>A	XP_011517007.1:p.Val344Glu
XM_005272200.3:c.917T>A	XP_005272257.1:p.Val306Glu
XM_011518705.2:c.1031T>A	XP_011517007.1:p.Val344Glu
XM_017014729.1:c.1013T>A	XP_016870218.1:p.Val338Glu
NM_054012.4:c.917T>A MANE Select	NP_446464.1:p.Val306Glu