Canonical Allele Identifier: CA467384872

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355772G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480385G>C , CM000671.2:g.130480385G>C	GRCh38
NC_000009.11:g.133355772G>C , CM000671.1:g.133355772G>C	GRCh37
NC_000009.10:g.132345593G>C	NCBI36
NG_011542.1:g.40679G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.774G>C MANE Select	ENSP00000253004.6:p.Ala258=
ENST00000352480.9:c.774G>C	ENSP00000253004.6:p.Ala258=
ENST00000372386.6:n.45G>C
ENST00000372393.7:c.774G>C	ENSP00000361469.2:p.Ala258=
ENST00000372394.5:c.774G>C	ENSP00000361471.1:p.Ala258=
ENST00000470849.4:n.499G>C
ENST00000492400.5:n.283G>C
ENST00000493984.6:n.551G>C
NM_000050.4:c.774G>C	NP_000041.2:p.Ala258=
NM_054012.3:c.774G>C	NP_446464.1:p.Ala258=
XM_005272200.2:c.774G>C	XP_005272257.1:p.Ala258=
XM_011518705.1:c.888G>C	XP_011517007.1:p.Ala296=
XM_005272200.3:c.774G>C	XP_005272257.1:p.Ala258=
XM_011518705.2:c.888G>C	XP_011517007.1:p.Ala296=
XM_017014729.1:c.870G>C	XP_016870218.1:p.Ala290=
NM_054012.4:c.774G>C MANE Select	NP_446464.1:p.Ala258=