Canonical Allele Identifier: CA450384022

Gene: POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43488056T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520318T>G , CM000668.2:g.43520318T>G	GRCh38
NC_000006.11:g.43488056T>G , CM000668.1:g.43488056T>G	GRCh37
NC_000006.10:g.43596034T>G	NCBI36
NG_028283.1:g.8280T>G
NG_028283.3:g.15617T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.546T>G	ENSP00000496683.1:p.Ala182=
ENST00000642195.1:c.546T>G MANE Select	ENSP00000496044.1:p.Ala182=
ENST00000643341.1:c.546T>G	ENSP00000496018.1:p.Ala182=
ENST00000643799.1:c.546T>G	ENSP00000494529.1:p.Ala182=
ENST00000645141.1:c.*157T>G	ENSP00000496755.1:n.*157T>G
ENST00000646188.1:c.381T>G	ENSP00000496001.1:p.Ala127=
ENST00000646433.1:c.546T>G	ENSP00000494368.1:p.Ala182=
ENST00000646700.1:c.546T>G	ENSP00000495521.1:p.Ala182=
ENST00000304004.7:c.546T>G	ENSP00000307212.3:p.Ala182=
ENST00000372344.6:c.546T>G	ENSP00000361419.2:p.Ala182=
ENST00000372389.7:c.546T>G	ENSP00000361465.3:p.Ala182=
ENST00000455605.2:n.839T>G
ENST00000481352.6:n.918T>G
ENST00000488601.6:n.785T>G
NM_203290.2:c.546T>G	NP_976035.1:p.Ala182=
XM_005249491.1:c.546T>G	XP_005249548.1:p.Ala182=
XM_011515000.1:c.546T>G	XP_011513302.1:p.Ala182=
NM_001318876.1:c.546T>G	NP_001305805.1:p.Ala182=
NM_001363658.1:c.546T>G	NP_001350587.1:p.Ala182=
NM_203290.3:c.546T>G	NP_976035.1:p.Ala182=
NM_203290.4:c.546T>G MANE Select	NP_976035.1:p.Ala182=
NM_001363658.2:c.546T>G	NP_001350587.1:p.Ala182=
NM_001318876.2:c.546T>G	NP_001305805.1:p.Ala182=