Canonical Allele Identifier: CA467385645

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364778C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489391C>G , CM000671.2:g.130489391C>G	GRCh38
NC_000009.11:g.133364778C>G , CM000671.1:g.133364778C>G	GRCh37
NC_000009.10:g.132354599C>G	NCBI36
NG_011542.1:g.49685C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.897C>G MANE Select	ENSP00000253004.6:p.Ala299=
ENST00000352480.9:c.897C>G	ENSP00000253004.6:p.Ala299=
ENST00000372386.6:n.168C>G
ENST00000372393.7:c.897C>G	ENSP00000361469.2:p.Ala299=
ENST00000372394.5:c.897C>G	ENSP00000361471.1:p.Ala299=
ENST00000470849.4:n.622C>G
ENST00000492400.5:n.406C>G
ENST00000493984.6:n.674C>G
NM_000050.4:c.897C>G	NP_000041.2:p.Ala299=
NM_054012.3:c.897C>G	NP_446464.1:p.Ala299=
XM_005272200.2:c.897C>G	XP_005272257.1:p.Ala299=
XM_011518705.1:c.1011C>G	XP_011517007.1:p.Ala337=
XM_005272200.3:c.897C>G	XP_005272257.1:p.Ala299=
XM_011518705.2:c.1011C>G	XP_011517007.1:p.Ala337=
XM_017014729.1:c.993C>G	XP_016870218.1:p.Ala331=
NM_054012.4:c.897C>G MANE Select	NP_446464.1:p.Ala299=