Canonical Allele Identifier: CA469790596

Gene: ERCC6 PGBD3

Linked Data

• MyVariant Identifiers: chr10:g.50732150T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524104T>A , CM000672.2:g.49524104T>A	GRCh38
NC_000010.10:g.50732150T>A , CM000672.1:g.50732150T>A	GRCh37
NC_000010.9:g.50402156T>A	NCBI36
NG_009442.1:g.19998A>T , LRG_465:g.19998A>T
NG_033155.1:g.5178A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1326A>T (ERCC6) MANE Select	ENSP00000348089.5:p.Gly442=
ENST00000447839.7:c.1326A>T (ERCC6) MANE Plus Clinical	ENSP00000387966.2:p.Gly442=
ENST00000679596.1:c.*955A>T (ERCC6)	ENSP00000504862.1:n.*955A>T
ENST00000679811.1:n.1409A>T (ERCC6)
ENST00000680107.1:c.652+4313A>T (ERCC6)	ENSP00000505909.1:n.652+4313A>T
ENST00000680233.1:n.1419A>T (ERCC6)
ENST00000681632.1:n.1404A>T (ERCC6)
ENST00000681659.1:c.1326A>T (ERCC6)	ENSP00000505631.1:p.Gly442=
ENST00000355832.9:c.1326A>T (ERCC6)	ENSP00000348089.5:p.Gly442=
ENST00000374127.3:c.-79A>T	ENSP00000363242.3:n.-79A>T
ENST00000447839.6:c.1326A>T	ENSP00000387966.2:p.Gly442=
ENST00000515869.1:c.1326A>T	ENSP00000423550.1:p.Gly442=
NM_000124.3:c.1326A>T (ERCC6)	NP_000115.1:p.Gly442=
NM_001277058.1:c.1326A>T	NP_001263987.1:p.Gly442=
NM_001277059.1:c.1326A>T	NP_001263988.1:p.Gly442=
NM_170753.3:c.-79A>T (PGBD3)	NP_736609.2:n.-79A>T
NM_001346440.1:c.1326A>T (ERCC6)	NP_001333369.1:p.Gly442=
NM_000124.4:c.1326A>T (ERCC6) MANE Select	NP_000115.1:p.Gly442=
NM_001277058.2:c.1326A>T (ERCC6) MANE Plus Clinical	NP_001263987.1:p.Gly442=
NM_001277059.2:c.1326A>T (ERCC6)	NP_001263988.1:p.Gly442=
NM_001346440.2:c.1326A>T (ERCC6)	NP_001333369.1:p.Gly442=