Canonical Allele Identifier: CA387298995

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425994G>T (hg19) ; chr12:g.131941449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941449G>T , CM000674.2:g.131941449G>T	GRCh38
NC_000012.11:g.132425994G>T , CM000674.1:g.132425994G>T	GRCh37
NC_000012.10:g.130991947G>T	NCBI36
NG_013039.1:g.17250G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.702G>T MANE Select	ENSP00000365837.3:p.Arg234Ser
ENST00000322060.9:c.618G>T	ENSP00000324726.5:p.Arg206Ser
ENST00000376649.7:c.702G>T	ENSP00000365837.3:p.Arg234Ser
ENST00000443358.6:c.618G>T	ENSP00000392451.2:p.Arg206Ser
ENST00000535067.5:c.358-2090G>T	ENSP00000443969.1:n.358-2090G>T
ENST00000542167.2:c.543G>T	ENSP00000438948.1:p.Arg181Ser
ENST00000543754.1:n.523G>T
NM_001002019.2:c.618G>T	NP_001002019.1:p.Arg206Ser
NM_001002020.2:c.618G>T	NP_001002020.1:p.Arg206Ser
NM_025215.5:c.702G>T	NP_079491.2:p.Arg234Ser
XM_011538768.1:c.303G>T	XP_011537070.1:p.Arg101Ser
XM_011538768.3:c.303G>T	XP_011537070.1:p.Arg101Ser
XR_001748872.1:n.1157G>T
NM_001002019.3:c.618G>T	NP_001002019.1:p.Arg206Ser
NM_001002020.3:c.618G>T	NP_001002020.1:p.Arg206Ser
NM_025215.6:c.702G>T MANE Select	NP_079491.2:p.Arg234Ser