Canonical Allele Identifier: CA375230489

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364743A>G (hg19) ; chr9:g.130489356A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489356A>G , CM000671.2:g.130489356A>G	GRCh38
NC_000009.11:g.133364743A>G , CM000671.1:g.133364743A>G	GRCh37
NC_000009.10:g.132354564A>G	NCBI36
NG_011542.1:g.49650A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.862A>G MANE Select	ENSP00000253004.6:p.Thr288Ala
ENST00000352480.9:c.862A>G	ENSP00000253004.6:p.Thr288Ala
ENST00000372386.6:n.133A>G
ENST00000372393.7:c.862A>G	ENSP00000361469.2:p.Thr288Ala
ENST00000372394.5:c.862A>G	ENSP00000361471.1:p.Thr288Ala
ENST00000470849.4:n.587A>G
ENST00000492400.5:n.371A>G
ENST00000493984.6:n.639A>G
NM_000050.4:c.862A>G	NP_000041.2:p.Thr288Ala
NM_054012.3:c.862A>G	NP_446464.1:p.Thr288Ala
XM_005272200.2:c.862A>G	XP_005272257.1:p.Thr288Ala
XM_011518705.1:c.976A>G	XP_011517007.1:p.Thr326Ala
XM_005272200.3:c.862A>G	XP_005272257.1:p.Thr288Ala
XM_011518705.2:c.976A>G	XP_011517007.1:p.Thr326Ala
XM_017014729.1:c.958A>G	XP_016870218.1:p.Thr320Ala
NM_054012.4:c.862A>G MANE Select	NP_446464.1:p.Thr288Ala