Canonical Allele Identifier: CA376754848

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732694C>G (hg19) ; chr10:g.49524648C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524648C>G , CM000672.2:g.49524648C>G	GRCh38
NC_000010.10:g.50732694C>G , CM000672.1:g.50732694C>G	GRCh37
NC_000010.9:g.50402700C>G	NCBI36
NG_009442.1:g.19454G>C , LRG_465:g.19454G>C
NG_033155.1:g.4634G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.782G>C MANE Select	ENSP00000348089.5:p.Arg261Thr
ENST00000447839.7:c.782G>C MANE Plus Clinical	ENSP00000387966.2:p.Arg261Thr
ENST00000679596.1:c.*411G>C	ENSP00000504862.1:n.*411G>C
ENST00000679811.1:n.865G>C
ENST00000680107.1:c.652+3769G>C	ENSP00000505909.1:n.652+3769G>C
ENST00000680233.1:n.875G>C
ENST00000681632.1:n.860G>C
ENST00000681659.1:c.782G>C	ENSP00000505631.1:p.Arg261Thr
ENST00000355832.9:c.782G>C	ENSP00000348089.5:p.Arg261Thr
ENST00000447839.6:c.782G>C	ENSP00000387966.2:p.Arg261Thr
ENST00000515869.1:c.782G>C	ENSP00000423550.1:p.Arg261Thr
NM_000124.3:c.782G>C	NP_000115.1:p.Arg261Thr
NM_001277058.1:c.782G>C	NP_001263987.1:p.Arg261Thr
NM_001277059.1:c.782G>C	NP_001263988.1:p.Arg261Thr
NM_001346440.1:c.782G>C	NP_001333369.1:p.Arg261Thr
NM_000124.4:c.782G>C MANE Select	NP_000115.1:p.Arg261Thr
NM_001277058.2:c.782G>C MANE Plus Clinical	NP_001263987.1:p.Arg261Thr
NM_001277059.2:c.782G>C	NP_001263988.1:p.Arg261Thr
NM_001346440.2:c.782G>C	NP_001333369.1:p.Arg261Thr