Canonical Allele Identifier: CA467388128

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133327640C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452253C>T , CM000671.2:g.130452253C>T	GRCh38
NC_000009.11:g.133327640C>T , CM000671.1:g.133327640C>T	GRCh37
NC_000009.10:g.132317461C>T	NCBI36
NG_011542.1:g.12547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.25C>T MANE Select	ENSP00000253004.6:p.Leu9=
ENST00000352480.9:c.25C>T	ENSP00000253004.6:p.Leu9=
ENST00000372393.7:c.25C>T	ENSP00000361469.2:p.Leu9=
ENST00000372394.5:c.25C>T	ENSP00000361471.1:p.Leu9=
ENST00000422569.5:c.25C>T	ENSP00000394212.1:p.Leu9=
ENST00000443588.1:c.25C>T	ENSP00000397785.1:p.Leu9=
NM_000050.4:c.25C>T	NP_000041.2:p.Leu9=
NM_054012.3:c.25C>T	NP_446464.1:p.Leu9=
XM_005272200.2:c.25C>T	XP_005272257.1:p.Leu9=
XM_011518705.1:c.139C>T	XP_011517007.1:p.Leu47=
XM_005272200.3:c.25C>T	XP_005272257.1:p.Leu9=
XM_011518705.2:c.139C>T	XP_011517007.1:p.Leu47=
XM_017014729.1:c.121C>T	XP_016870218.1:p.Leu41=
NM_054012.4:c.25C>T MANE Select	NP_446464.1:p.Leu9=