Canonical Allele Identifier: CA376714121

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470437-C-T
• COSMIC: COSM1348068
• MyVariant Identifiers: chr10:g.50678483C>T (hg19) ; chr10:g.49470437C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470437C>T , CM000672.2:g.49470437C>T	GRCh38
NC_000010.10:g.50678483C>T , CM000672.1:g.50678483C>T	GRCh37
NC_000010.9:g.50348489C>T	NCBI36
NG_009442.1:g.73665G>A , LRG_465:g.73665G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3523G>A MANE Select	ENSP00000348089.5:p.Glu1175Lys
ENST00000679552.1:n.594G>A
ENST00000679871.1:n.669G>A
ENST00000679974.1:n.572G>A
ENST00000681632.1:n.4926G>A
ENST00000681659.1:c.3364G>A	ENSP00000505631.1:p.Glu1122Lys
ENST00000355832.9:c.3523G>A	ENSP00000348089.5:p.Glu1175Lys
ENST00000623073.3:c.*1819G>A	ENSP00000485650.1:n.*1819G>A
ENST00000623115.3:c.1633G>A	ENSP00000485321.1:p.Glu545Lys
ENST00000624341.3:c.1355G>A
NM_000124.3:c.3523G>A	NP_000115.1:p.Glu1175Lys
XR_945953.1:n.243-1128C>T
NM_001346440.1:c.3523G>A	NP_001333369.1:p.Glu1175Lys
NM_000124.4:c.3523G>A MANE Select	NP_000115.1:p.Glu1175Lys
NM_001346440.2:c.3523G>A	NP_001333369.1:p.Glu1175Lys