Canonical Allele Identifier: CA375230860

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364847T>G (hg19) ; chr9:g.130489460T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489460T>G , CM000671.2:g.130489460T>G	GRCh38
NC_000009.11:g.133364847T>G , CM000671.1:g.133364847T>G	GRCh37
NC_000009.10:g.132354668T>G	NCBI36
NG_011542.1:g.49754T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.966T>G MANE Select	ENSP00000253004.6:p.Tyr322Ter
ENST00000352480.9:c.966T>G	ENSP00000253004.6:p.Tyr322Ter
ENST00000372386.6:n.237T>G
ENST00000372393.7:c.966T>G	ENSP00000361469.2:p.Tyr322Ter
ENST00000372394.5:c.966T>G	ENSP00000361471.1:p.Tyr322Ter
NM_000050.4:c.966T>G	NP_000041.2:p.Tyr322Ter
NM_054012.3:c.966T>G	NP_446464.1:p.Tyr322Ter
XM_005272200.2:c.966T>G	XP_005272257.1:p.Tyr322Ter
XM_011518705.1:c.1080T>G	XP_011517007.1:p.Tyr360Ter
XM_005272200.3:c.966T>G	XP_005272257.1:p.Tyr322Ter
XM_011518705.2:c.1080T>G	XP_011517007.1:p.Tyr360Ter
XM_017014729.1:c.1062T>G	XP_016870218.1:p.Tyr354Ter
NM_054012.4:c.966T>G MANE Select	NP_446464.1:p.Tyr322Ter