Canonical Allele Identifier: CA387299121

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132426052C>A (hg19) ; chr12:g.131941507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941507C>A , CM000674.2:g.131941507C>A	GRCh38
NC_000012.11:g.132426052C>A , CM000674.1:g.132426052C>A	GRCh37
NC_000012.10:g.130992005C>A	NCBI36
NG_013039.1:g.17308C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.760C>A MANE Select	ENSP00000365837.3:p.Pro254Thr
ENST00000322060.9:c.676C>A	ENSP00000324726.5:p.Pro226Thr
ENST00000376649.7:c.760C>A	ENSP00000365837.3:p.Pro254Thr
ENST00000443358.6:c.676C>A	ENSP00000392451.2:p.Pro226Thr
ENST00000535067.5:c.358-2032C>A	ENSP00000443969.1:n.358-2032C>A
ENST00000542167.2:c.601C>A	ENSP00000438948.1:p.Pro201Thr
ENST00000543754.1:n.581C>A
NM_001002019.2:c.676C>A	NP_001002019.1:p.Pro226Thr
NM_001002020.2:c.676C>A	NP_001002020.1:p.Pro226Thr
NM_025215.5:c.760C>A	NP_079491.2:p.Pro254Thr
XM_011538768.1:c.361C>A	XP_011537070.1:p.Pro121Thr
XM_011538768.3:c.361C>A	XP_011537070.1:p.Pro121Thr
XR_001748872.1:n.1215C>A
NM_001002019.3:c.676C>A	NP_001002019.1:p.Pro226Thr
NM_001002020.3:c.676C>A	NP_001002020.1:p.Pro226Thr
NM_025215.6:c.760C>A MANE Select	NP_079491.2:p.Pro254Thr