Canonical Allele Identifier: CA450290483

Gene: POLR1C

Linked Data

• gnomAD v3: 6-43520686-C-T
• gnomAD v4: 6-43520686-C-T
• MyVariant Identifiers: chr6:g.43488424C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520686C>T , CM000668.2:g.43520686C>T	GRCh38
NC_000006.11:g.43488424C>T , CM000668.1:g.43488424C>T	GRCh37
NC_000006.10:g.43596402C>T	NCBI36
NG_028283.1:g.8648C>T
NG_028283.3:g.15985C>T
NG_051658.1:g.60390G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.717C>T	ENSP00000496683.1:p.Ile239=
ENST00000642195.1:c.717C>T MANE Select	ENSP00000496044.1:p.Ile239=
ENST00000643341.1:c.717C>T	ENSP00000496018.1:p.Ile239=
ENST00000643799.1:c.656-246C>T	ENSP00000494529.1:n.656-246C>T
ENST00000645141.1:c.*328C>T	ENSP00000496755.1:n.*328C>T
ENST00000646188.1:c.552C>T	ENSP00000496001.1:p.Ile184=
ENST00000646433.1:c.717C>T	ENSP00000494368.1:p.Ile239=
ENST00000646700.1:c.717C>T	ENSP00000495521.1:p.Ile239=
ENST00000304004.7:c.717C>T	ENSP00000307212.3:p.Ile239=
ENST00000372344.6:c.656-246C>T	ENSP00000361419.2:n.656-246C>T
ENST00000372389.7:c.717C>T	ENSP00000361465.3:p.Ile239=
ENST00000455605.2:n.1207C>T
ENST00000481352.6:n.1089C>T
ENST00000488601.6:n.956C>T
NM_203290.2:c.717C>T	NP_976035.1:p.Ile239=
XM_005249491.1:c.717C>T	XP_005249548.1:p.Ile239=
XM_011515000.1:c.717C>T	XP_011513302.1:p.Ile239=
NM_001318876.1:c.717C>T	NP_001305805.1:p.Ile239=
NM_001363658.1:c.717C>T	NP_001350587.1:p.Ile239=
NM_203290.3:c.717C>T	NP_976035.1:p.Ile239=
NM_203290.4:c.717C>T MANE Select	NP_976035.1:p.Ile239=
NM_001363658.2:c.717C>T	NP_001350587.1:p.Ile239=
NM_001318876.2:c.717C>T	NP_001305805.1:p.Ile239=