Canonical Allele Identifier: CA387298771

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425888G>T (hg19) ; chr12:g.131941343G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941343G>T , CM000674.2:g.131941343G>T	GRCh38
NC_000012.11:g.132425888G>T , CM000674.1:g.132425888G>T	GRCh37
NC_000012.10:g.130991841G>T	NCBI36
NG_013039.1:g.17144G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.596G>T MANE Select	ENSP00000365837.3:p.Arg199Met
ENST00000322060.9:c.512G>T	ENSP00000324726.5:p.Arg171Met
ENST00000376649.7:c.596G>T	ENSP00000365837.3:p.Arg199Met
ENST00000443358.6:c.512G>T	ENSP00000392451.2:p.Arg171Met
ENST00000535067.5:c.358-2196G>T	ENSP00000443969.1:n.358-2196G>T
ENST00000537484.1:c.521G>T	ENSP00000440179.1:p.Arg174Met
ENST00000542167.2:c.437G>T	ENSP00000438948.1:p.Arg146Met
ENST00000543754.1:n.417G>T
NM_001002019.2:c.512G>T	NP_001002019.1:p.Arg171Met
NM_001002020.2:c.512G>T	NP_001002020.1:p.Arg171Met
NM_025215.5:c.596G>T	NP_079491.2:p.Arg199Met
XM_011538768.1:c.197G>T	XP_011537070.1:p.Arg66Met
XM_011538768.3:c.197G>T	XP_011537070.1:p.Arg66Met
XR_001748872.1:n.1051G>T
NM_001002019.3:c.512G>T	NP_001002019.1:p.Arg171Met
NM_001002020.3:c.512G>T	NP_001002020.1:p.Arg171Met
NM_025215.6:c.596G>T MANE Select	NP_079491.2:p.Arg199Met