Canonical Allele Identifier: CA375230855

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364846A>T (hg19) ; chr9:g.130489459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489459A>T , CM000671.2:g.130489459A>T	GRCh38
NC_000009.11:g.133364846A>T , CM000671.1:g.133364846A>T	GRCh37
NC_000009.10:g.132354667A>T	NCBI36
NG_011542.1:g.49753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.965A>T MANE Select	ENSP00000253004.6:p.Tyr322Phe
ENST00000352480.9:c.965A>T	ENSP00000253004.6:p.Tyr322Phe
ENST00000372386.6:n.236A>T
ENST00000372393.7:c.965A>T	ENSP00000361469.2:p.Tyr322Phe
ENST00000372394.5:c.965A>T	ENSP00000361471.1:p.Tyr322Phe
NM_000050.4:c.965A>T	NP_000041.2:p.Tyr322Phe
NM_054012.3:c.965A>T	NP_446464.1:p.Tyr322Phe
XM_005272200.2:c.965A>T	XP_005272257.1:p.Tyr322Phe
XM_011518705.1:c.1079A>T	XP_011517007.1:p.Tyr360Phe
XM_005272200.3:c.965A>T	XP_005272257.1:p.Tyr322Phe
XM_011518705.2:c.1079A>T	XP_011517007.1:p.Tyr360Phe
XM_017014729.1:c.1061A>T	XP_016870218.1:p.Tyr354Phe
NM_054012.4:c.965A>T MANE Select	NP_446464.1:p.Tyr322Phe