Canonical Allele Identifier: CA376741548

Gene: ERCC6 PGBD3

Linked Data

• MyVariant Identifiers: chr10:g.50724332A>T (hg19) ; chr10:g.49516286A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49516286A>T , CM000672.2:g.49516286A>T	GRCh38
NC_000010.10:g.50724332A>T , CM000672.1:g.50724332A>T	GRCh37
NC_000010.9:g.50394338A>T	NCBI36
NG_009442.1:g.27816T>A , LRG_465:g.27816T>A
NG_033155.1:g.12996T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1397+7747T>A (ERCC6) MANE Select	ENSP00000348089.5:n.1397+7747T>A
ENST00000447839.7:c.2233T>A (ERCC6) MANE Plus Clinical	ENSP00000387966.2:p.Phe745Ile
ENST00000679596.1:c.*1862T>A (ERCC6)	ENSP00000504862.1:n.*1862T>A
ENST00000679811.1:n.1480+7747T>A (ERCC6)
ENST00000680107.1:c.*813T>A (ERCC6)	ENSP00000505909.1:n.*813T>A
ENST00000681632.1:n.1475+7747T>A (ERCC6)
ENST00000681659.1:c.1397+7747T>A (ERCC6)	ENSP00000505631.1:n.1397+7747T>A
ENST00000355832.9:c.1397+7747T>A (ERCC6)	ENSP00000348089.5:n.1397+7747T>A
ENST00000374127.3:c.829T>A	ENSP00000363242.3:p.Phe277Ile
ENST00000447839.6:c.2233T>A	ENSP00000387966.2:p.Phe745Ile
ENST00000515869.1:c.2233T>A	ENSP00000423550.1:p.Phe745Ile
NM_000124.3:c.1397+7747T>A (ERCC6)	NP_000115.1:n.1397+7747T>A
NM_001277058.1:c.2233T>A	NP_001263987.1:p.Phe745Ile
NM_001277059.1:c.2233T>A	NP_001263988.1:p.Phe745Ile
NM_170753.3:c.829T>A (PGBD3)	NP_736609.2:p.Phe277Ile
NM_001346440.1:c.1397+7747T>A (ERCC6)	NP_001333369.1:n.1397+7747T>A
NM_000124.4:c.1397+7747T>A (ERCC6) MANE Select	NP_000115.1:n.1397+7747T>A
NM_001277058.2:c.2233T>A (ERCC6) MANE Plus Clinical	NP_001263987.1:p.Phe745Ile
NM_001277059.2:c.2233T>A (ERCC6)	NP_001263988.1:p.Phe745Ile
NM_001346440.2:c.1397+7747T>A (ERCC6)	NP_001333369.1:n.1397+7747T>A