Canonical Allele Identifier: CA376724288

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50690810C>T (hg19) ; chr10:g.49482764C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482764C>T , CM000672.2:g.49482764C>T	GRCh38
NC_000010.10:g.50690810C>T , CM000672.1:g.50690810C>T	GRCh37
NC_000010.9:g.50360816C>T	NCBI36
NG_009442.1:g.61338G>A , LRG_465:g.61338G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2092G>A MANE Select	ENSP00000348089.5:p.Gly698Ser
ENST00000681632.1:n.2170G>A
ENST00000681659.1:c.1933G>A	ENSP00000505631.1:p.Gly645Ser
ENST00000355832.9:c.2092G>A	ENSP00000348089.5:p.Gly698Ser
ENST00000623073.3:c.*484G>A	ENSP00000485650.1:n.*484G>A
ENST00000623115.3:c.202G>A	ENSP00000485321.1:p.Gly68Ser
NM_000124.3:c.2092G>A	NP_000115.1:p.Gly698Ser
NM_001346440.1:c.2092G>A	NP_001333369.1:p.Gly698Ser
NM_000124.4:c.2092G>A MANE Select	NP_000115.1:p.Gly698Ser
NM_001346440.2:c.2092G>A	NP_001333369.1:p.Gly698Ser