Canonical Allele Identifier: CA376716164

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678761G>T (hg19) ; chr10:g.49470715G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470715G>T , CM000672.2:g.49470715G>T	GRCh38
NC_000010.10:g.50678761G>T , CM000672.1:g.50678761G>T	GRCh37
NC_000010.9:g.50348767G>T	NCBI36
NG_009442.1:g.73387C>A , LRG_465:g.73387C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3245C>A MANE Select	ENSP00000348089.5:p.Ala1082Glu
ENST00000679552.1:n.316C>A
ENST00000679871.1:n.391C>A
ENST00000679974.1:n.294C>A
ENST00000681632.1:n.4648C>A
ENST00000681659.1:c.3086C>A	ENSP00000505631.1:p.Ala1029Glu
ENST00000355832.9:c.3245C>A	ENSP00000348089.5:p.Ala1082Glu
ENST00000623073.3:c.*1541C>A	ENSP00000485650.1:n.*1541C>A
ENST00000623115.3:c.1355C>A	ENSP00000485321.1:p.Ala452Glu
ENST00000624341.3:c.1077C>A
NM_000124.3:c.3245C>A	NP_000115.1:p.Ala1082Glu
XR_945953.1:n.243-850G>T
NM_001346440.1:c.3245C>A	NP_001333369.1:p.Ala1082Glu
NM_000124.4:c.3245C>A MANE Select	NP_000115.1:p.Ala1082Glu
NM_001346440.2:c.3245C>A	NP_001333369.1:p.Ala1082Glu