Canonical Allele Identifier: CA7583502
Community Standard Title: NM_015532.5(POLR2M):c.526C>T (p.Arg176Cys)
Gene: POLR2M HGNC NCBI
GCOM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.57709126C>T , CM000677.2:g.57709126C>T GRCh38
NC_000015.9:g.58001324C>T , CM000677.1:g.58001324C>T GRCh37
NC_000015.8:g.55788616C>T NCBI36
NG_029676.1:g.7424C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015532.5:c.526C>T (POLR2M) MANE Select NP_056347.1:p.Arg176Cys
ENST00000299638.8:c.526C>T (POLR2M) MANE Select ENSP00000299638.3:p.Arg176Cys
NM_001018090.6:c.1305-2858C>T (GCOM1) NP_001018100.1:n.1305-2858C>T
NM_001018091.6:c.1305-5410C>T (GCOM1) NP_001018101.1:n.1305-5410C>T
NM_001018102.2:c.114-59C>T (POLR2M) NP_001018112.1:n.114-59C>T
NM_001018102.3:c.114-59C>T (POLR2M) NP_001018112.1:n.114-59C>T
NM_001285900.3:c.1717C>T (GCOM1) NP_001272829.1:p.Arg573Cys
NM_015532.4:c.526C>T (POLR2M) NP_056347.1:p.Arg176Cys
NR_104367.2:n.2215-2858C>T (GCOM1)
NR_104368.2:n.1409-2858C>T (GCOM1)
NR_104369.2:n.1335-2858C>T (GCOM1)
NR_104370.2:n.1251-2858C>T (GCOM1)
NR_104371.3:n.2638C>T (GCOM1)
ENST00000299638.7:c.526C>T (POLR2M) ENSP00000299638.3:p.Arg176Cys
ENST00000380557.4:c.114-59C>T (POLR2M) ENSP00000369930.4:n.114-59C>T
ENST00000380568.7:c.1305-5410C>T (GCOM1) ENSP00000369942.3:n.1305-5410C>T
ENST00000380569.6:c.1305-2858C>T (GCOM1) ENSP00000369943.2:n.1305-2858C>T
ENST00000460962.5:c.*1190C>T (GCOM1) ENSP00000435774.1:n.*1190C>T
ENST00000463717.5:c.*33-2858C>T (GCOM1) ENSP00000435028.1:n.*33-2858C>T
ENST00000464277.1:c.*595C>T (POLR2M) ENSP00000437015.1:n.*595C>T
ENST00000464277.2:c.*595C>T (POLR2M) ENSP00000437015.3:n.*595C>T
ENST00000464308.1:n.536C>T (POLR2M)
ENST00000477282.5:c.1120-2858C>T (GCOM1) ENSP00000434505.1:n.1120-2858C>T
ENST00000482814.5:c.1204-2858C>T (GCOM1) ENSP00000436922.1:n.1204-2858C>T
ENST00000482852.5:c.526C>T (POLR2M) ENSP00000432615.1:p.Arg176Cys
ENST00000484300.1:n.367-59C>T (GCOM1)
ENST00000494490.1:c.*599C>T (POLR2M) ENSP00000433988.1:n.*599C>T
ENST00000494490.2:c.*599C>T (POLR2M) ENSP00000433988.3:n.*599C>T
ENST00000496627.5:c.*911-2858C>T (GCOM1) ENSP00000436614.1:n.*911-2858C>T
ENST00000587652.5:c.1717C>T (GCOM1) ENSP00000465231.1:p.Arg573Cys