Canonical Allele Identifier: CA375225747

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133339498G>C (hg19) ; chr9:g.130464111G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130464111G>C , CM000671.2:g.130464111G>C	GRCh38
NC_000009.11:g.133339498G>C , CM000671.1:g.133339498G>C	GRCh37
NC_000009.10:g.132329319G>C	NCBI36
NG_011542.1:g.24405G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.364G>C MANE Select	ENSP00000253004.6:p.Gly122Arg
ENST00000352480.9:c.364G>C	ENSP00000253004.6:p.Gly122Arg
ENST00000372393.7:c.364G>C	ENSP00000361469.2:p.Gly122Arg
ENST00000372394.5:c.364G>C	ENSP00000361471.1:p.Gly122Arg
ENST00000422569.5:c.364G>C	ENSP00000394212.1:p.Gly122Arg
ENST00000443588.1:c.364-2614G>C	ENSP00000397785.1:n.364-2614G>C
ENST00000467695.5:n.73G>C
NM_000050.4:c.364G>C	NP_000041.2:p.Gly122Arg
NM_054012.3:c.364G>C	NP_446464.1:p.Gly122Arg
XM_005272200.2:c.364G>C	XP_005272257.1:p.Gly122Arg
XM_011518705.1:c.478G>C	XP_011517007.1:p.Gly160Arg
XM_005272200.3:c.364G>C	XP_005272257.1:p.Gly122Arg
XM_011518705.2:c.478G>C	XP_011517007.1:p.Gly160Arg
XM_017014729.1:c.460G>C	XP_016870218.1:p.Gly154Arg
NM_054012.4:c.364G>C MANE Select	NP_446464.1:p.Gly122Arg