Canonical Allele Identifier: CA376754402

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732627A>T (hg19) ; chr10:g.49524581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524581A>T , CM000672.2:g.49524581A>T	GRCh38
NC_000010.10:g.50732627A>T , CM000672.1:g.50732627A>T	GRCh37
NC_000010.9:g.50402633A>T	NCBI36
NG_009442.1:g.19521T>A , LRG_465:g.19521T>A
NG_033155.1:g.4701T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.849T>A MANE Select	ENSP00000348089.5:p.Phe283Leu
ENST00000447839.7:c.849T>A MANE Plus Clinical	ENSP00000387966.2:p.Phe283Leu
ENST00000679596.1:c.*478T>A	ENSP00000504862.1:n.*478T>A
ENST00000679811.1:n.932T>A
ENST00000680107.1:c.652+3836T>A	ENSP00000505909.1:n.652+3836T>A
ENST00000680233.1:n.942T>A
ENST00000681632.1:n.927T>A
ENST00000681659.1:c.849T>A	ENSP00000505631.1:p.Phe283Leu
ENST00000355832.9:c.849T>A	ENSP00000348089.5:p.Phe283Leu
ENST00000447839.6:c.849T>A	ENSP00000387966.2:p.Phe283Leu
ENST00000515869.1:c.849T>A	ENSP00000423550.1:p.Phe283Leu
NM_000124.3:c.849T>A	NP_000115.1:p.Phe283Leu
NM_001277058.1:c.849T>A	NP_001263987.1:p.Phe283Leu
NM_001277059.1:c.849T>A	NP_001263988.1:p.Phe283Leu
NM_001346440.1:c.849T>A	NP_001333369.1:p.Phe283Leu
NM_000124.4:c.849T>A MANE Select	NP_000115.1:p.Phe283Leu
NM_001277058.2:c.849T>A MANE Plus Clinical	NP_001263987.1:p.Phe283Leu
NM_001277059.2:c.849T>A	NP_001263988.1:p.Phe283Leu
NM_001346440.2:c.849T>A	NP_001333369.1:p.Phe283Leu