Canonical Allele Identifier: CA469600286

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669433G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461387G>C , CM000672.2:g.49461387G>C	GRCh38
NC_000010.10:g.50669433G>C , CM000672.1:g.50669433G>C	GRCh37
NC_000010.9:g.50339439G>C	NCBI36
NG_009442.1:g.82715C>G , LRG_465:g.82715C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3948C>G MANE Select	ENSP00000348089.5:p.Gly1316=
ENST00000679552.1:n.1019C>G
ENST00000679871.1:n.1094C>G
ENST00000679974.1:n.997C>G
ENST00000681632.1:n.5351C>G
ENST00000681659.1:c.3789C>G	ENSP00000505631.1:p.Gly1263=
ENST00000355832.9:c.3948C>G	ENSP00000348089.5:p.Gly1316=
ENST00000465653.1:n.270C>G
ENST00000623073.3:c.*2244C>G	ENSP00000485650.1:n.*2244C>G
ENST00000623115.3:c.2058C>G	ENSP00000485321.1:p.Gly686=
ENST00000624341.3:c.1780C>G
NM_000124.3:c.3948C>G	NP_000115.1:p.Gly1316=
XR_945953.1:n.243-10178G>C
NM_001346440.1:c.3948C>G	NP_001333369.1:p.Gly1316=
NM_000124.4:c.3948C>G MANE Select	NP_000115.1:p.Gly1316=
NM_001346440.2:c.3948C>G	NP_001333369.1:p.Gly1316=