Canonical Allele Identifier: CA467384899

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355790C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480403C>T , CM000671.2:g.130480403C>T	GRCh38
NC_000009.11:g.133355790C>T , CM000671.1:g.133355790C>T	GRCh37
NC_000009.10:g.132345611C>T	NCBI36
NG_011542.1:g.40697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.792C>T MANE Select	ENSP00000253004.6:p.Gly264=
ENST00000352480.9:c.792C>T	ENSP00000253004.6:p.Gly264=
ENST00000372386.6:n.63C>T
ENST00000372393.7:c.792C>T	ENSP00000361469.2:p.Gly264=
ENST00000372394.5:c.792C>T	ENSP00000361471.1:p.Gly264=
ENST00000470849.4:n.517C>T
ENST00000492400.5:n.301C>T
ENST00000493984.6:n.569C>T
NM_000050.4:c.792C>T	NP_000041.2:p.Gly264=
NM_054012.3:c.792C>T	NP_446464.1:p.Gly264=
XM_005272200.2:c.792C>T	XP_005272257.1:p.Gly264=
XM_011518705.1:c.906C>T	XP_011517007.1:p.Gly302=
XM_005272200.3:c.792C>T	XP_005272257.1:p.Gly264=
XM_011518705.2:c.906C>T	XP_011517007.1:p.Gly302=
XM_017014729.1:c.888C>T	XP_016870218.1:p.Gly296=
NM_054012.4:c.792C>T MANE Select	NP_446464.1:p.Gly264=