Canonical Allele Identifier: CA376726400
Gene: ERCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493122T>G , CM000672.2:g.49493122T>G GRCh38
NC_000010.10:g.50701168T>G , CM000672.1:g.50701168T>G GRCh37
NC_000010.9:g.50371174T>G NCBI36
NG_009442.1:g.50980A>C , LRG_465:g.50980A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1816A>C MANE Select ENSP00000348089.5:p.Lys606Gln
ENST00000681632.1:n.1894A>C
ENST00000681659.1:c.1657A>C ENSP00000505631.1:p.Lys553Gln
ENST00000355832.9:c.1816A>C ENSP00000348089.5:p.Lys606Gln
ENST00000475116.1:n.275+7416A>C
ENST00000623073.3:c.217A>C ENSP00000485650.1:p.Lys73Gln
ENST00000623115.3:c.-70+7416A>C ENSP00000485321.1:n.-70+7416A>C
ENST00000623318.1:c.217A>C ENSP00000485423.1:p.Lys73Gln
NM_000124.3:c.1816A>C NP_000115.1:p.Lys606Gln
NM_001346440.1:c.1816A>C NP_001333369.1:p.Lys606Gln
NM_000124.4:c.1816A>C MANE Select NP_000115.1:p.Lys606Gln
NM_001346440.2:c.1816A>C NP_001333369.1:p.Lys606Gln