Canonical Allele Identifier: CA376716987

Gene: ERCC6

Linked Data

• COSMIC: COSM13871
• MyVariant Identifiers: chr10:g.50678893C>G (hg19) ; chr10:g.49470847C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470847C>G , CM000672.2:g.49470847C>G	GRCh38
NC_000010.10:g.50678893C>G , CM000672.1:g.50678893C>G	GRCh37
NC_000010.9:g.50348899C>G	NCBI36
NG_009442.1:g.73255G>C , LRG_465:g.73255G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3113G>C MANE Select	ENSP00000348089.5:p.Arg1038Thr
ENST00000679552.1:n.184G>C
ENST00000679871.1:n.259G>C
ENST00000679974.1:n.162G>C
ENST00000681632.1:n.4516G>C
ENST00000681659.1:c.2954G>C	ENSP00000505631.1:p.Arg985Thr
ENST00000355832.9:c.3113G>C	ENSP00000348089.5:p.Arg1038Thr
ENST00000623073.3:c.*1409G>C	ENSP00000485650.1:n.*1409G>C
ENST00000623115.3:c.1223G>C	ENSP00000485321.1:p.Arg408Thr
ENST00000624341.3:c.945G>C
NM_000124.3:c.3113G>C	NP_000115.1:p.Arg1038Thr
XR_945953.1:n.243-718C>G
NM_001346440.1:c.3113G>C	NP_001333369.1:p.Arg1038Thr
NM_000124.4:c.3113G>C MANE Select	NP_000115.1:p.Arg1038Thr
NM_001346440.2:c.3113G>C	NP_001333369.1:p.Arg1038Thr