Canonical Allele Identifier: CA450383991

Gene: POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43488014G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520276G>C , CM000668.2:g.43520276G>C	GRCh38
NC_000006.11:g.43488014G>C , CM000668.1:g.43488014G>C	GRCh37
NC_000006.10:g.43595992G>C	NCBI36
NG_028283.1:g.8238G>C
NG_028283.3:g.15575G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.504G>C	ENSP00000496683.1:p.Val168=
ENST00000642195.1:c.504G>C MANE Select	ENSP00000496044.1:p.Val168=
ENST00000643341.1:c.504G>C	ENSP00000496018.1:p.Val168=
ENST00000643799.1:c.504G>C	ENSP00000494529.1:p.Val168=
ENST00000645141.1:c.*115G>C	ENSP00000496755.1:n.*115G>C
ENST00000646188.1:c.339G>C	ENSP00000496001.1:p.Val113=
ENST00000646433.1:c.504G>C	ENSP00000494368.1:p.Val168=
ENST00000646700.1:c.504G>C	ENSP00000495521.1:p.Val168=
ENST00000304004.7:c.504G>C	ENSP00000307212.3:p.Val168=
ENST00000372344.6:c.504G>C	ENSP00000361419.2:p.Val168=
ENST00000372389.7:c.504G>C	ENSP00000361465.3:p.Val168=
ENST00000423780.1:c.382G>C
ENST00000428025.6:c.339G>C	ENSP00000395401.2:p.Val113=
ENST00000455605.2:n.797G>C
ENST00000481352.6:n.876G>C
ENST00000488601.6:n.743G>C
NM_203290.2:c.504G>C	NP_976035.1:p.Val168=
XM_005249491.1:c.504G>C	XP_005249548.1:p.Val168=
XM_011515000.1:c.504G>C	XP_011513302.1:p.Val168=
NM_001318876.1:c.504G>C	NP_001305805.1:p.Val168=
NM_001363658.1:c.504G>C	NP_001350587.1:p.Val168=
NM_203290.3:c.504G>C	NP_976035.1:p.Val168=
NM_203290.4:c.504G>C MANE Select	NP_976035.1:p.Val168=
NM_001363658.2:c.504G>C	NP_001350587.1:p.Val168=
NM_001318876.2:c.504G>C	NP_001305805.1:p.Val168=