Canonical Allele Identifier: CA376752879

Gene: ERCC6

Linked Data

• COSMIC: COSM918676
• MyVariant Identifiers: chr10:g.50732357C>A (hg19) ; chr10:g.49524311C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524311C>A , CM000672.2:g.49524311C>A	GRCh38
NC_000010.10:g.50732357C>A , CM000672.1:g.50732357C>A	GRCh37
NC_000010.9:g.50402363C>A	NCBI36
NG_009442.1:g.19791G>T , LRG_465:g.19791G>T
NG_033155.1:g.4971G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1119G>T MANE Select	ENSP00000348089.5:p.Glu373Asp
ENST00000447839.7:c.1119G>T MANE Plus Clinical	ENSP00000387966.2:p.Glu373Asp
ENST00000679596.1:c.*748G>T	ENSP00000504862.1:n.*748G>T
ENST00000679811.1:n.1202G>T
ENST00000680107.1:c.652+4106G>T	ENSP00000505909.1:n.652+4106G>T
ENST00000680233.1:n.1212G>T
ENST00000681632.1:n.1197G>T
ENST00000681659.1:c.1119G>T	ENSP00000505631.1:p.Glu373Asp
ENST00000355832.9:c.1119G>T	ENSP00000348089.5:p.Glu373Asp
ENST00000447839.6:c.1119G>T	ENSP00000387966.2:p.Glu373Asp
ENST00000515869.1:c.1119G>T	ENSP00000423550.1:p.Glu373Asp
NM_000124.3:c.1119G>T	NP_000115.1:p.Glu373Asp
NM_001277058.1:c.1119G>T	NP_001263987.1:p.Glu373Asp
NM_001277059.1:c.1119G>T	NP_001263988.1:p.Glu373Asp
NM_001346440.1:c.1119G>T	NP_001333369.1:p.Glu373Asp
NM_000124.4:c.1119G>T MANE Select	NP_000115.1:p.Glu373Asp
NM_001277058.2:c.1119G>T MANE Plus Clinical	NP_001263987.1:p.Glu373Asp
NM_001277059.2:c.1119G>T	NP_001263988.1:p.Glu373Asp
NM_001346440.2:c.1119G>T	NP_001333369.1:p.Glu373Asp