Canonical Allele Identifier: CA467384893

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355787G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480400G>T , CM000671.2:g.130480400G>T	GRCh38
NC_000009.11:g.133355787G>T , CM000671.1:g.133355787G>T	GRCh37
NC_000009.10:g.132345608G>T	NCBI36
NG_011542.1:g.40694G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.789G>T MANE Select	ENSP00000253004.6:p.Val263=
ENST00000352480.9:c.789G>T	ENSP00000253004.6:p.Val263=
ENST00000372386.6:n.60G>T
ENST00000372393.7:c.789G>T	ENSP00000361469.2:p.Val263=
ENST00000372394.5:c.789G>T	ENSP00000361471.1:p.Val263=
ENST00000470849.4:n.514G>T
ENST00000492400.5:n.298G>T
ENST00000493984.6:n.566G>T
NM_000050.4:c.789G>T	NP_000041.2:p.Val263=
NM_054012.3:c.789G>T	NP_446464.1:p.Val263=
XM_005272200.2:c.789G>T	XP_005272257.1:p.Val263=
XM_011518705.1:c.903G>T	XP_011517007.1:p.Val301=
XM_005272200.3:c.789G>T	XP_005272257.1:p.Val263=
XM_011518705.2:c.903G>T	XP_011517007.1:p.Val301=
XM_017014729.1:c.885G>T	XP_016870218.1:p.Val295=
NM_054012.4:c.789G>T MANE Select	NP_446464.1:p.Val263=