Canonical Allele Identifier: CA1624559365

Gene: POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520411C= , CM000668.2:g.43520411C=	GRCh38
NC_000006.11:g.43488149C= , CM000668.1:g.43488149C=	GRCh37
NC_000006.10:g.43596127C=	NCBI36
NG_028283.1:g.8373C=
NG_028283.3:g.15710C=
NG_051658.1:g.60665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.639C=	ENSP00000496683.1:p.His213=
ENST00000642195.1:c.639C= MANE Select	ENSP00000496044.1:p.His213=
ENST00000643341.1:c.639C=	ENSP00000496018.1:p.His213=
ENST00000643799.1:c.639C=	ENSP00000494529.1:p.His213=
ENST00000645141.1:c.*250C=	ENSP00000496755.1:n.*250C=
ENST00000646188.1:c.474C=	ENSP00000496001.1:p.His158=
ENST00000646433.1:c.639C=	ENSP00000494368.1:p.His213=
ENST00000646700.1:c.639C=	ENSP00000495521.1:p.His213=
ENST00000304004.7:c.639C=	ENSP00000307212.3:p.His213=
ENST00000372344.6:c.639C=	ENSP00000361419.2:p.His213=
ENST00000372389.7:c.639C=	ENSP00000361465.3:p.His213=
ENST00000455605.2:n.932C=
ENST00000481352.6:n.1011C=
ENST00000488601.6:n.878C=
NM_203290.2:c.639C=	NP_976035.1:p.His213=
XM_005249491.1:c.639C=	XP_005249548.1:p.His213=
XM_011515000.1:c.639C=	XP_011513302.1:p.His213=
NM_001318876.1:c.639C=	NP_001305805.1:p.His213=
NM_001363658.1:c.639C=	NP_001350587.1:p.His213=
NM_203290.3:c.639C=	NP_976035.1:p.His213=
NM_203290.4:c.639C= MANE Select	NP_976035.1:p.His213=
NM_001363658.2:c.639C=	NP_001350587.1:p.His213=
NM_001318876.2:c.639C=	NP_001305805.1:p.His213=