Canonical Allele Identifier: CA376713240

Gene: ERCC6

Linked Data

• COSMIC: COSM4014440
• MyVariant Identifiers: chr10:g.50678377T>G (hg19) ; chr10:g.49470331T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470331T>G , CM000672.2:g.49470331T>G	GRCh38
NC_000010.10:g.50678377T>G , CM000672.1:g.50678377T>G	GRCh37
NC_000010.9:g.50348383T>G	NCBI36
NG_009442.1:g.73771A>C , LRG_465:g.73771A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3629A>C MANE Select	ENSP00000348089.5:p.Lys1210Thr
ENST00000679552.1:n.700A>C
ENST00000679871.1:n.775A>C
ENST00000679974.1:n.678A>C
ENST00000681632.1:n.5032A>C
ENST00000681659.1:c.3470A>C	ENSP00000505631.1:p.Lys1157Thr
ENST00000355832.9:c.3629A>C	ENSP00000348089.5:p.Lys1210Thr
ENST00000623073.3:c.*1925A>C	ENSP00000485650.1:n.*1925A>C
ENST00000623115.3:c.1739A>C	ENSP00000485321.1:p.Lys580Thr
ENST00000624341.3:c.1461A>C
NM_000124.3:c.3629A>C	NP_000115.1:p.Lys1210Thr
XR_945953.1:n.243-1234T>G
NM_001346440.1:c.3629A>C	NP_001333369.1:p.Lys1210Thr
NM_000124.4:c.3629A>C MANE Select	NP_000115.1:p.Lys1210Thr
NM_001346440.2:c.3629A>C	NP_001333369.1:p.Lys1210Thr