Canonical Allele Identifier: CA450287212

Gene: GTPBP2 POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43590376A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43622639A>G , CM000668.2:g.43622639A>G	GRCh38
NC_000006.11:g.43590376A>G , CM000668.1:g.43590376A>G	GRCh37
NC_000006.10:g.43698354A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307126.10:c.1461T>C (GTPBP2) MANE Select	ENSP00000303997.5:p.Leu487=
ENST00000307114.11:c.1197T>C (GTPBP2)	ENSP00000304893.7:p.Leu399=
ENST00000307126.9:c.1461T>C (GTPBP2)	ENSP00000303997.5:p.Leu487=
ENST00000419497.5:c.166T>C (GTPBP2)
ENST00000432918.5:c.166T>C (GTPBP2)
ENST00000476510.5:n.1344T>C (GTPBP2)
NM_001286216.1:c.1197T>C (GTPBP2)	NP_001273145.1:p.Leu399=
NM_019096.4:c.1461T>C (GTPBP2)	NP_061969.3:p.Leu487=
XM_017010976.1:c.1461T>C (GTPBP2)	XP_016866465.1:p.Leu487=
XM_024446475.1:c.1317T>C (GTPBP2)	XP_024302243.1:p.Leu439=
XM_024446476.1:c.1317T>C (GTPBP2)	XP_024302244.1:p.Leu439=
XM_024446477.1:c.1197T>C (GTPBP2)	XP_024302245.1:p.Leu399=
XM_024446478.1:c.1197T>C (GTPBP2)	XP_024302246.1:p.Leu399=
NM_019096.5:c.1461T>C (GTPBP2) MANE Select	NP_061969.3:p.Leu487=
NM_001286216.2:c.1197T>C (GTPBP2)	NP_001273145.1:p.Leu399=
NM_001318876.2:c.945+93368A>G (POLR1C)	NP_001305805.1:n.945+93368A>G