Canonical Allele Identifier: CA376729219

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50708733C>A (hg19) ; chr10:g.49500687C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500687C>A , CM000672.2:g.49500687C>A	GRCh38
NC_000010.10:g.50708733C>A , CM000672.1:g.50708733C>A	GRCh37
NC_000010.9:g.50378739C>A	NCBI36
NG_009442.1:g.43415G>T , LRG_465:g.43415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1536G>T MANE Select	ENSP00000348089.5:p.Gln512His
ENST00000681632.1:n.1614G>T
ENST00000681659.1:c.1526+5197G>T	ENSP00000505631.1:n.1526+5197G>T
ENST00000355832.9:c.1536G>T	ENSP00000348089.5:p.Gln512His
ENST00000475116.1:n.126G>T
ENST00000623073.3:c.-64G>T	ENSP00000485650.1:n.-64G>T
ENST00000623115.3:c.-219G>T	ENSP00000485321.1:n.-219G>T
ENST00000623318.1:c.-64G>T	ENSP00000485423.1:n.-64G>T
ENST00000623788.1:n.535G>T
NM_000124.3:c.1536G>T	NP_000115.1:p.Gln512His
NM_001346440.1:c.1536G>T	NP_001333369.1:p.Gln512His
NM_000124.4:c.1536G>T MANE Select	NP_000115.1:p.Gln512His
NM_001346440.2:c.1536G>T	NP_001333369.1:p.Gln512His