Canonical Allele Identifier: CA376713003

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678345G>C (hg19) ; chr10:g.49470299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470299G>C , CM000672.2:g.49470299G>C	GRCh38
NC_000010.10:g.50678345G>C , CM000672.1:g.50678345G>C	GRCh37
NC_000010.9:g.50348351G>C	NCBI36
NG_009442.1:g.73803C>G , LRG_465:g.73803C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3661C>G MANE Select	ENSP00000348089.5:p.Arg1221Gly
ENST00000679552.1:n.732C>G
ENST00000679871.1:n.807C>G
ENST00000679974.1:n.710C>G
ENST00000681632.1:n.5064C>G
ENST00000681659.1:c.3502C>G	ENSP00000505631.1:p.Arg1168Gly
ENST00000355832.9:c.3661C>G	ENSP00000348089.5:p.Arg1221Gly
ENST00000623073.3:c.*1957C>G	ENSP00000485650.1:n.*1957C>G
ENST00000623115.3:c.1771C>G	ENSP00000485321.1:p.Arg591Gly
ENST00000624341.3:c.1493C>G
NM_000124.3:c.3661C>G	NP_000115.1:p.Arg1221Gly
XR_945953.1:n.243-1266G>C
NM_001346440.1:c.3661C>G	NP_001333369.1:p.Arg1221Gly
NM_000124.4:c.3661C>G MANE Select	NP_000115.1:p.Arg1221Gly
NM_001346440.2:c.3661C>G	NP_001333369.1:p.Arg1221Gly