Canonical Allele Identifier: CA2678869134

Gene: POLR1C

Linked Data

• gnomAD v4: 6-43519869-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43519869C>T , CM000668.2:g.43519869C>T	GRCh38
NC_000006.11:g.43487607C>T , CM000668.1:g.43487607C>T	GRCh37
NC_000006.10:g.43595585C>T	NCBI36
NG_028283.1:g.7831C>T
NG_028283.3:g.15168C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.382+31C>T	ENSP00000496683.1:n.382+31C>T
ENST00000642195.1:c.382+31C>T MANE Select	ENSP00000496044.1:n.382+31C>T
ENST00000643341.1:c.382+31C>T	ENSP00000496018.1:n.382+31C>T
ENST00000643799.1:c.382+31C>T	ENSP00000494529.1:n.382+31C>T
ENST00000645141.1:c.413C>T	ENSP00000496755.1:p.Thr138Ile
ENST00000646188.1:c.217+31C>T	ENSP00000496001.1:n.217+31C>T
ENST00000646433.1:c.382+31C>T	ENSP00000494368.1:n.382+31C>T
ENST00000646700.1:c.382+31C>T	ENSP00000495521.1:n.382+31C>T
ENST00000304004.7:c.382+31C>T	ENSP00000307212.3:n.382+31C>T
ENST00000372344.6:c.382+31C>T	ENSP00000361419.2:n.382+31C>T
ENST00000372389.7:c.382+31C>T	ENSP00000361465.3:n.382+31C>T
ENST00000423780.1:c.380+31C>T
ENST00000428025.6:c.217+31C>T	ENSP00000395401.2:n.217+31C>T
ENST00000455605.2:n.390C>T
ENST00000481352.6:n.469C>T
ENST00000488601.6:n.425C>T
NM_203290.2:c.382+31C>T	NP_976035.1:n.382+31C>T
XM_005249491.1:c.382+31C>T	XP_005249548.1:n.382+31C>T
XM_011515000.1:c.382+31C>T	XP_011513302.1:n.382+31C>T
NM_001318876.1:c.382+31C>T	NP_001305805.1:n.382+31C>T
NM_001363658.1:c.382+31C>T	NP_001350587.1:n.382+31C>T
NM_203290.3:c.382+31C>T	NP_976035.1:n.382+31C>T
NM_203290.4:c.382+31C>T MANE Select	NP_976035.1:n.382+31C>T
NM_001363658.2:c.382+31C>T	NP_001350587.1:n.382+31C>T
NM_001318876.2:c.382+31C>T	NP_001305805.1:n.382+31C>T