Canonical Allele Identifier: CA375230579

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364783C>G (hg19) ; chr9:g.130489396C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489396C>G , CM000671.2:g.130489396C>G	GRCh38
NC_000009.11:g.133364783C>G , CM000671.1:g.133364783C>G	GRCh37
NC_000009.10:g.132354604C>G	NCBI36
NG_011542.1:g.49690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.902C>G MANE Select	ENSP00000253004.6:p.Thr301Ser
ENST00000352480.9:c.902C>G	ENSP00000253004.6:p.Thr301Ser
ENST00000372386.6:n.173C>G
ENST00000372393.7:c.902C>G	ENSP00000361469.2:p.Thr301Ser
ENST00000372394.5:c.902C>G	ENSP00000361471.1:p.Thr301Ser
ENST00000470849.4:n.627C>G
ENST00000492400.5:n.411C>G
ENST00000493984.6:n.679C>G
NM_000050.4:c.902C>G	NP_000041.2:p.Thr301Ser
NM_054012.3:c.902C>G	NP_446464.1:p.Thr301Ser
XM_005272200.2:c.902C>G	XP_005272257.1:p.Thr301Ser
XM_011518705.1:c.1016C>G	XP_011517007.1:p.Thr339Ser
XM_005272200.3:c.902C>G	XP_005272257.1:p.Thr301Ser
XM_011518705.2:c.1016C>G	XP_011517007.1:p.Thr339Ser
XM_017014729.1:c.998C>G	XP_016870218.1:p.Thr333Ser
NM_054012.4:c.902C>G MANE Select	NP_446464.1:p.Thr301Ser