Canonical Allele Identifier: CA375223504

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133327641T>G (hg19) ; chr9:g.130452254T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452254T>G , CM000671.2:g.130452254T>G	GRCh38
NC_000009.11:g.133327641T>G , CM000671.1:g.133327641T>G	GRCh37
NC_000009.10:g.132317462T>G	NCBI36
NG_011542.1:g.12548T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.26T>G MANE Select	ENSP00000253004.6:p.Leu9Arg
ENST00000352480.9:c.26T>G	ENSP00000253004.6:p.Leu9Arg
ENST00000372393.7:c.26T>G	ENSP00000361469.2:p.Leu9Arg
ENST00000372394.5:c.26T>G	ENSP00000361471.1:p.Leu9Arg
ENST00000422569.5:c.26T>G	ENSP00000394212.1:p.Leu9Arg
ENST00000443588.1:c.26T>G	ENSP00000397785.1:p.Leu9Arg
NM_000050.4:c.26T>G	NP_000041.2:p.Leu9Arg
NM_054012.3:c.26T>G	NP_446464.1:p.Leu9Arg
XM_005272200.2:c.26T>G	XP_005272257.1:p.Leu9Arg
XM_011518705.1:c.140T>G	XP_011517007.1:p.Leu47Arg
XM_005272200.3:c.26T>G	XP_005272257.1:p.Leu9Arg
XM_011518705.2:c.140T>G	XP_011517007.1:p.Leu47Arg
XM_017014729.1:c.122T>G	XP_016870218.1:p.Leu41Arg
NM_054012.4:c.26T>G MANE Select	NP_446464.1:p.Leu9Arg