Canonical Allele Identifier: CA387299079

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132426033T>G (hg19) ; chr12:g.131941488T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941488T>G , CM000674.2:g.131941488T>G	GRCh38
NC_000012.11:g.132426033T>G , CM000674.1:g.132426033T>G	GRCh37
NC_000012.10:g.130991986T>G	NCBI36
NG_013039.1:g.17289T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.741T>G MANE Select	ENSP00000365837.3:p.Asn247Lys
ENST00000322060.9:c.657T>G	ENSP00000324726.5:p.Asn219Lys
ENST00000376649.7:c.741T>G	ENSP00000365837.3:p.Asn247Lys
ENST00000443358.6:c.657T>G	ENSP00000392451.2:p.Asn219Lys
ENST00000535067.5:c.358-2051T>G	ENSP00000443969.1:n.358-2051T>G
ENST00000542167.2:c.582T>G	ENSP00000438948.1:p.Asn194Lys
ENST00000543754.1:n.562T>G
NM_001002019.2:c.657T>G	NP_001002019.1:p.Asn219Lys
NM_001002020.2:c.657T>G	NP_001002020.1:p.Asn219Lys
NM_025215.5:c.741T>G	NP_079491.2:p.Asn247Lys
XM_011538768.1:c.342T>G	XP_011537070.1:p.Asn114Lys
XM_011538768.3:c.342T>G	XP_011537070.1:p.Asn114Lys
XR_001748872.1:n.1196T>G
NM_001002019.3:c.657T>G	NP_001002019.1:p.Asn219Lys
NM_001002020.3:c.657T>G	NP_001002020.1:p.Asn219Lys
NM_025215.6:c.741T>G MANE Select	NP_079491.2:p.Asn247Lys