Canonical Allele Identifier: CA376714751

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678559T>G (hg19) ; chr10:g.49470513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470513T>G , CM000672.2:g.49470513T>G	GRCh38
NC_000010.10:g.50678559T>G , CM000672.1:g.50678559T>G	GRCh37
NC_000010.9:g.50348565T>G	NCBI36
NG_009442.1:g.73589A>C , LRG_465:g.73589A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3447A>C MANE Select	ENSP00000348089.5:p.Glu1149Asp
ENST00000679552.1:n.518A>C
ENST00000679871.1:n.593A>C
ENST00000679974.1:n.496A>C
ENST00000681632.1:n.4850A>C
ENST00000681659.1:c.3288A>C	ENSP00000505631.1:p.Glu1096Asp
ENST00000355832.9:c.3447A>C	ENSP00000348089.5:p.Glu1149Asp
ENST00000623073.3:c.*1743A>C	ENSP00000485650.1:n.*1743A>C
ENST00000623115.3:c.1557A>C	ENSP00000485321.1:p.Glu519Asp
ENST00000624341.3:c.1279A>C
NM_000124.3:c.3447A>C	NP_000115.1:p.Glu1149Asp
XR_945953.1:n.243-1052T>G
NM_001346440.1:c.3447A>C	NP_001333369.1:p.Glu1149Asp
NM_000124.4:c.3447A>C MANE Select	NP_000115.1:p.Glu1149Asp
NM_001346440.2:c.3447A>C	NP_001333369.1:p.Glu1149Asp