Canonical Allele Identifier: CA467384939

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355823A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480436A>G , CM000671.2:g.130480436A>G	GRCh38
NC_000009.11:g.133355823A>G , CM000671.1:g.133355823A>G	GRCh37
NC_000009.10:g.132345644A>G	NCBI36
NG_011542.1:g.40730A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.825A>G MANE Select	ENSP00000253004.6:p.Gly275=
ENST00000352480.9:c.825A>G	ENSP00000253004.6:p.Gly275=
ENST00000372386.6:n.96A>G
ENST00000372393.7:c.825A>G	ENSP00000361469.2:p.Gly275=
ENST00000372394.5:c.825A>G	ENSP00000361471.1:p.Gly275=
ENST00000470849.4:n.550A>G
ENST00000492400.5:n.334A>G
ENST00000493984.6:n.602A>G
NM_000050.4:c.825A>G	NP_000041.2:p.Gly275=
NM_054012.3:c.825A>G	NP_446464.1:p.Gly275=
XM_005272200.2:c.825A>G	XP_005272257.1:p.Gly275=
XM_011518705.1:c.939A>G	XP_011517007.1:p.Gly313=
XM_005272200.3:c.825A>G	XP_005272257.1:p.Gly275=
XM_011518705.2:c.939A>G	XP_011517007.1:p.Gly313=
XM_017014729.1:c.921A>G	XP_016870218.1:p.Gly307=
NM_054012.4:c.825A>G MANE Select	NP_446464.1:p.Gly275=