Canonical Allele Identifier: CA1908760321

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482769T= , CM000672.2:g.49482769T=	GRCh38
NC_000010.10:g.50690815T= , CM000672.1:g.50690815T=	GRCh37
NC_000010.9:g.50360821T=	NCBI36
NG_009442.1:g.61333A= , LRG_465:g.61333A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2087A= MANE Select	ENSP00000348089.5:p.Lys696=
ENST00000681632.1:n.2165A=
ENST00000681659.1:c.1928A=	ENSP00000505631.1:p.Lys643=
ENST00000355832.9:c.2087A=	ENSP00000348089.5:p.Lys696=
ENST00000623073.3:c.*479A=	ENSP00000485650.1:n.*479A=
ENST00000623115.3:c.197A=	ENSP00000485321.1:p.Lys66=
NM_000124.3:c.2087A=	NP_000115.1:p.Lys696=
NM_001346440.1:c.2087A=	NP_001333369.1:p.Lys696=
NM_000124.4:c.2087A= MANE Select	NP_000115.1:p.Lys696=
NM_001346440.2:c.2087A=	NP_001333369.1:p.Lys696=