Canonical Allele Identifier: CA376708534

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669543C>T (hg19) ; chr10:g.49461497C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461497C>T , CM000672.2:g.49461497C>T	GRCh38
NC_000010.10:g.50669543C>T , CM000672.1:g.50669543C>T	GRCh37
NC_000010.9:g.50339549C>T	NCBI36
NG_009442.1:g.82605G>A , LRG_465:g.82605G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3838G>A MANE Select	ENSP00000348089.5:p.Val1280Ile
ENST00000679552.1:n.909G>A
ENST00000679871.1:n.984G>A
ENST00000679974.1:n.887G>A
ENST00000681632.1:n.5241G>A
ENST00000681659.1:c.3679G>A	ENSP00000505631.1:p.Val1227Ile
ENST00000355832.9:c.3838G>A	ENSP00000348089.5:p.Val1280Ile
ENST00000465653.1:n.160G>A
ENST00000623073.3:c.*2134G>A	ENSP00000485650.1:n.*2134G>A
ENST00000623115.3:c.1948G>A	ENSP00000485321.1:p.Val650Ile
ENST00000624341.3:c.1670G>A
NM_000124.3:c.3838G>A	NP_000115.1:p.Val1280Ile
XR_945953.1:n.243-10068C>T
NM_001346440.1:c.3838G>A	NP_001333369.1:p.Val1280Ile
NM_000124.4:c.3838G>A MANE Select	NP_000115.1:p.Val1280Ile
NM_001346440.2:c.3838G>A	NP_001333369.1:p.Val1280Ile