Canonical Allele Identifier: CA376716397

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678798C>G (hg19) ; chr10:g.49470752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470752C>G , CM000672.2:g.49470752C>G	GRCh38
NC_000010.10:g.50678798C>G , CM000672.1:g.50678798C>G	GRCh37
NC_000010.9:g.50348804C>G	NCBI36
NG_009442.1:g.73350G>C , LRG_465:g.73350G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3208G>C MANE Select	ENSP00000348089.5:p.Glu1070Gln
ENST00000679552.1:n.279G>C
ENST00000679871.1:n.354G>C
ENST00000679974.1:n.257G>C
ENST00000681632.1:n.4611G>C
ENST00000681659.1:c.3049G>C	ENSP00000505631.1:p.Glu1017Gln
ENST00000355832.9:c.3208G>C	ENSP00000348089.5:p.Glu1070Gln
ENST00000623073.3:c.*1504G>C	ENSP00000485650.1:n.*1504G>C
ENST00000623115.3:c.1318G>C	ENSP00000485321.1:p.Glu440Gln
ENST00000624341.3:c.1040G>C
NM_000124.3:c.3208G>C	NP_000115.1:p.Glu1070Gln
XR_945953.1:n.243-813C>G
NM_001346440.1:c.3208G>C	NP_001333369.1:p.Glu1070Gln
NM_000124.4:c.3208G>C MANE Select	NP_000115.1:p.Glu1070Gln
NM_001346440.2:c.3208G>C	NP_001333369.1:p.Glu1070Gln