Canonical Allele Identifier: CA375230754

Gene: ASS1

Linked Data

• COSMIC: COSM1314566
• MyVariant Identifiers: chr9:g.133364826G>C (hg19) ; chr9:g.130489439G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489439G>C , CM000671.2:g.130489439G>C	GRCh38
NC_000009.11:g.133364826G>C , CM000671.1:g.133364826G>C	GRCh37
NC_000009.10:g.132354647G>C	NCBI36
NG_011542.1:g.49733G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.945G>C MANE Select	ENSP00000253004.6:p.Leu315Phe
ENST00000352480.9:c.945G>C	ENSP00000253004.6:p.Leu315Phe
ENST00000372386.6:n.216G>C
ENST00000372393.7:c.945G>C	ENSP00000361469.2:p.Leu315Phe
ENST00000372394.5:c.945G>C	ENSP00000361471.1:p.Leu315Phe
NM_000050.4:c.945G>C	NP_000041.2:p.Leu315Phe
NM_054012.3:c.945G>C	NP_446464.1:p.Leu315Phe
XM_005272200.2:c.945G>C	XP_005272257.1:p.Leu315Phe
XM_011518705.1:c.1059G>C	XP_011517007.1:p.Leu353Phe
XM_005272200.3:c.945G>C	XP_005272257.1:p.Leu315Phe
XM_011518705.2:c.1059G>C	XP_011517007.1:p.Leu353Phe
XM_017014729.1:c.1041G>C	XP_016870218.1:p.Leu347Phe
NM_054012.4:c.945G>C MANE Select	NP_446464.1:p.Leu315Phe