Canonical Allele Identifier: CA450290692

Gene: POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43488484T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520746T>G , CM000668.2:g.43520746T>G	GRCh38
NC_000006.11:g.43488484T>G , CM000668.1:g.43488484T>G	GRCh37
NC_000006.10:g.43596462T>G	NCBI36
NG_028283.1:g.8708T>G
NG_028283.3:g.16045T>G
NG_051658.1:g.60330A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.777T>G	ENSP00000496683.1:p.Pro259=
ENST00000642195.1:c.777T>G MANE Select	ENSP00000496044.1:p.Pro259=
ENST00000643341.1:c.777T>G	ENSP00000496018.1:p.Pro259=
ENST00000643799.1:c.656-186T>G	ENSP00000494529.1:n.656-186T>G
ENST00000645141.1:c.*388T>G	ENSP00000496755.1:n.*388T>G
ENST00000646188.1:c.612T>G	ENSP00000496001.1:p.Pro204=
ENST00000646433.1:c.777T>G	ENSP00000494368.1:p.Pro259=
ENST00000646700.1:c.777T>G	ENSP00000495521.1:p.Pro259=
ENST00000304004.7:c.777T>G	ENSP00000307212.3:p.Pro259=
ENST00000372344.6:c.656-186T>G	ENSP00000361419.2:n.656-186T>G
ENST00000372389.7:c.777T>G	ENSP00000361465.3:p.Pro259=
ENST00000455605.2:n.1267T>G
ENST00000481352.6:n.1149T>G
NM_203290.2:c.777T>G	NP_976035.1:p.Pro259=
XM_005249491.1:c.777T>G	XP_005249548.1:p.Pro259=
XM_011515000.1:c.777T>G	XP_011513302.1:p.Pro259=
NM_001318876.1:c.777T>G	NP_001305805.1:p.Pro259=
NM_001363658.1:c.777T>G	NP_001350587.1:p.Pro259=
NM_203290.3:c.777T>G	NP_976035.1:p.Pro259=
NM_203290.4:c.777T>G MANE Select	NP_976035.1:p.Pro259=
NM_001363658.2:c.777T>G	NP_001350587.1:p.Pro259=
NM_001318876.2:c.777T>G	NP_001305805.1:p.Pro259=