Canonical Allele Identifier: CA387298854

Gene: PUS1

Linked Data

• dbSNP Id: rs1566147770
• gnomAD v2: 12-132425926-C-T
• gnomAD v3: 12-131941381-C-T
• gnomAD v4: 12-131941381-C-T
• MyVariant Identifiers: chr12:g.132425926C>T (hg19) ; chr12:g.131941381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941381C>T , CM000674.2:g.131941381C>T	GRCh38
NC_000012.11:g.132425926C>T , CM000674.1:g.132425926C>T	GRCh37
NC_000012.10:g.130991879C>T	NCBI36
NG_013039.1:g.17182C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.634C>T MANE Select	ENSP00000365837.3:p.His212Tyr
ENST00000322060.9:c.550C>T	ENSP00000324726.5:p.His184Tyr
ENST00000376649.7:c.634C>T	ENSP00000365837.3:p.His212Tyr
ENST00000443358.6:c.550C>T	ENSP00000392451.2:p.His184Tyr
ENST00000535067.5:c.358-2158C>T	ENSP00000443969.1:n.358-2158C>T
ENST00000537484.1:c.559C>T	ENSP00000440179.1:p.His187Tyr
ENST00000542167.2:c.475C>T	ENSP00000438948.1:p.His159Tyr
ENST00000543754.1:n.455C>T
NM_001002019.2:c.550C>T	NP_001002019.1:p.His184Tyr
NM_001002020.2:c.550C>T	NP_001002020.1:p.His184Tyr
NM_025215.5:c.634C>T	NP_079491.2:p.His212Tyr
XM_011538768.1:c.235C>T	XP_011537070.1:p.His79Tyr
XM_011538768.3:c.235C>T	XP_011537070.1:p.His79Tyr
XR_001748872.1:n.1089C>T
NM_001002019.3:c.550C>T	NP_001002019.1:p.His184Tyr
NM_001002020.3:c.550C>T	NP_001002020.1:p.His184Tyr
NM_025215.6:c.634C>T MANE Select	NP_079491.2:p.His212Tyr