Canonical Allele Identifier: CA375230476

Gene: ASS1

Linked Data

• COSMIC: COSM1460494 ; COSM5830966
• MyVariant Identifiers: chr9:g.133364737G>A (hg19) ; chr9:g.130489350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489350G>A , CM000671.2:g.130489350G>A	GRCh38
NC_000009.11:g.133364737G>A , CM000671.1:g.133364737G>A	GRCh37
NC_000009.10:g.132354558G>A	NCBI36
NG_011542.1:g.49644G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.856G>A MANE Select	ENSP00000253004.6:p.Ala286Thr
ENST00000352480.9:c.856G>A	ENSP00000253004.6:p.Ala286Thr
ENST00000372386.6:n.127G>A
ENST00000372393.7:c.856G>A	ENSP00000361469.2:p.Ala286Thr
ENST00000372394.5:c.856G>A	ENSP00000361471.1:p.Ala286Thr
ENST00000470849.4:n.581G>A
ENST00000492400.5:n.365G>A
ENST00000493984.6:n.633G>A
NM_000050.4:c.856G>A	NP_000041.2:p.Ala286Thr
NM_054012.3:c.856G>A	NP_446464.1:p.Ala286Thr
XM_005272200.2:c.856G>A	XP_005272257.1:p.Ala286Thr
XM_011518705.1:c.970G>A	XP_011517007.1:p.Ala324Thr
XM_005272200.3:c.856G>A	XP_005272257.1:p.Ala286Thr
XM_011518705.2:c.970G>A	XP_011517007.1:p.Ala324Thr
XM_017014729.1:c.952G>A	XP_016870218.1:p.Ala318Thr
NM_054012.4:c.856G>A MANE Select	NP_446464.1:p.Ala286Thr