Canonical Allele Identifier: CA376714389

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678519C>T (hg19) ; chr10:g.49470473C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470473C>T , CM000672.2:g.49470473C>T	GRCh38
NC_000010.10:g.50678519C>T , CM000672.1:g.50678519C>T	GRCh37
NC_000010.9:g.50348525C>T	NCBI36
NG_009442.1:g.73629G>A , LRG_465:g.73629G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3487G>A MANE Select	ENSP00000348089.5:p.Ala1163Thr
ENST00000679552.1:n.558G>A
ENST00000679871.1:n.633G>A
ENST00000679974.1:n.536G>A
ENST00000681632.1:n.4890G>A
ENST00000681659.1:c.3328G>A	ENSP00000505631.1:p.Ala1110Thr
ENST00000355832.9:c.3487G>A	ENSP00000348089.5:p.Ala1163Thr
ENST00000623073.3:c.*1783G>A	ENSP00000485650.1:n.*1783G>A
ENST00000623115.3:c.1597G>A	ENSP00000485321.1:p.Ala533Thr
ENST00000624341.3:c.1319G>A
NM_000124.3:c.3487G>A	NP_000115.1:p.Ala1163Thr
XR_945953.1:n.243-1092C>T
NM_001346440.1:c.3487G>A	NP_001333369.1:p.Ala1163Thr
NM_000124.4:c.3487G>A MANE Select	NP_000115.1:p.Ala1163Thr
NM_001346440.2:c.3487G>A	NP_001333369.1:p.Ala1163Thr