Canonical Allele Identifier: CA387634789
Gene: POLR1D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27622916G>A , CM000675.2:g.27622916G>A GRCh38
NC_000013.10:g.28197053G>A , CM000675.1:g.28197053G>A GRCh37
NC_000013.9:g.27095053G>A NCBI36
NG_028908.1:g.7174G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000636952.2:c.26+907G>A ENSP00000508561.1:n.26+907G>A
ENST00000685267.1:c.26+907G>A ENSP00000508576.1:n.26+907G>A
ENST00000692944.1:c.26+907G>A ENSP00000510286.1:n.26+907G>A
ENST00000693488.1:c.-59+1479G>A ENSP00000508846.1:n.-59+1479G>A
ENST00000302979.5:c.68G>A MANE Select ENSP00000302478.4:p.Arg23Lys
ENST00000636817.1:c.26+907G>A ENSP00000490310.1:n.26+907G>A
ENST00000637071.1:c.-84+907G>A ENSP00000489713.1:n.-84+907G>A
ENST00000637180.1:c.-59+1479G>A ENSP00000490619.1:n.-59+1479G>A
ENST00000637389.1:n.71+1653G>A
ENST00000302979.4:c.68G>A ENSP00000302478.3:p.Arg23Lys
ENST00000399696.3:c.17G>A ENSP00000382603.2:p.Arg6Lys
ENST00000399697.7:c.26+907G>A ENSP00000382604.3:n.26+907G>A
ENST00000465887.2:c.26+907G>A ENSP00000487057.1:n.26+907G>A
ENST00000489647.4:c.26+907G>A ENSP00000483656.1:n.26+907G>A
ENST00000621089.2:c.-59+1776G>A ENSP00000478213.1:n.-59+1776G>A
ENST00000627604.1:c.-59+1479G>A ENSP00000486327.1:n.-59+1479G>A
ENST00000630983.1:c.26+907G>A ENSP00000486928.1:n.26+907G>A
NM_001206559.1:c.-59+1776G>A NP_001193488.1:n.-59+1776G>A
NM_015972.3:c.68G>A NP_057056.1:p.Arg23Lys
NM_152705.2:c.26+907G>A NP_689918.1:n.26+907G>A
XM_005266412.1:c.68G>A XP_005266469.1:p.Arg23Lys
XM_005266414.1:c.26+907G>A XP_005266471.1:n.26+907G>A
XM_005266412.2:c.68G>A XP_005266469.1:p.Arg23Lys
NM_001206559.2:c.-59+1776G>A NP_001193488.1:n.-59+1776G>A
NM_001374407.1:c.68G>A NP_001361336.1:p.Arg23Lys
NM_015972.4:c.68G>A MANE Select NP_057056.1:p.Arg23Lys
NM_152705.3:c.26+907G>A NP_689918.1:n.26+907G>A