Canonical Allele Identifier: CA387298978

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425986G>A (hg19) ; chr12:g.131941441G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941441G>A , CM000674.2:g.131941441G>A	GRCh38
NC_000012.11:g.132425986G>A , CM000674.1:g.132425986G>A	GRCh37
NC_000012.10:g.130991939G>A	NCBI36
NG_013039.1:g.17242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.694G>A MANE Select	ENSP00000365837.3:p.Val232Ile
ENST00000322060.9:c.610G>A	ENSP00000324726.5:p.Val204Ile
ENST00000376649.7:c.694G>A	ENSP00000365837.3:p.Val232Ile
ENST00000443358.6:c.610G>A	ENSP00000392451.2:p.Val204Ile
ENST00000535067.5:c.358-2098G>A	ENSP00000443969.1:n.358-2098G>A
ENST00000542167.2:c.535G>A	ENSP00000438948.1:p.Val179Ile
ENST00000543754.1:n.515G>A
NM_001002019.2:c.610G>A	NP_001002019.1:p.Val204Ile
NM_001002020.2:c.610G>A	NP_001002020.1:p.Val204Ile
NM_025215.5:c.694G>A	NP_079491.2:p.Val232Ile
XM_011538768.1:c.295G>A	XP_011537070.1:p.Val99Ile
XM_011538768.3:c.295G>A	XP_011537070.1:p.Val99Ile
XR_001748872.1:n.1149G>A
NM_001002019.3:c.610G>A	NP_001002019.1:p.Val204Ile
NM_001002020.3:c.610G>A	NP_001002020.1:p.Val204Ile
NM_025215.6:c.694G>A MANE Select	NP_079491.2:p.Val232Ile