Canonical Allele Identifier: CA375224775

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133333789T>G (hg19) ; chr9:g.130458402T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130458402T>G , CM000671.2:g.130458402T>G	GRCh38
NC_000009.11:g.133333789T>G , CM000671.1:g.133333789T>G	GRCh37
NC_000009.10:g.132323610T>G	NCBI36
NG_011542.1:g.18696T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.176T>G MANE Select	ENSP00000253004.6:p.Val59Gly
ENST00000352480.9:c.176T>G	ENSP00000253004.6:p.Val59Gly
ENST00000372393.7:c.176T>G	ENSP00000361469.2:p.Val59Gly
ENST00000372394.5:c.176T>G	ENSP00000361471.1:p.Val59Gly
ENST00000422569.5:c.176T>G	ENSP00000394212.1:p.Val59Gly
ENST00000443588.1:c.176T>G	ENSP00000397785.1:p.Val59Gly
NM_000050.4:c.176T>G	NP_000041.2:p.Val59Gly
NM_054012.3:c.176T>G	NP_446464.1:p.Val59Gly
XM_005272200.2:c.176T>G	XP_005272257.1:p.Val59Gly
XM_011518705.1:c.290T>G	XP_011517007.1:p.Val97Gly
XM_005272200.3:c.176T>G	XP_005272257.1:p.Val59Gly
XM_011518705.2:c.290T>G	XP_011517007.1:p.Val97Gly
XM_017014729.1:c.272T>G	XP_016870218.1:p.Val91Gly
NM_054012.4:c.176T>G MANE Select	NP_446464.1:p.Val59Gly