Canonical Allele Identifier: CA1908780795

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49505883C= , CM000672.2:g.49505883C=	GRCh38
NC_000010.10:g.50713929C= , CM000672.1:g.50713929C=	GRCh37
NC_000010.9:g.50383935C=	NCBI36
NG_009442.1:g.38219G= , LRG_465:g.38219G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000124.4:c.1526+1G= MANE Select	NP_000115.1:n.1526+1G=
ENST00000355832.10:c.1526+1G= MANE Select	ENSP00000348089.5:n.1526+1G=
NM_000124.3:c.1526+1G=	NP_000115.1:n.1526+1G=
NM_001346440.1:c.1526+1G=	NP_001333369.1:n.1526+1G=
NM_001346440.2:c.1526+1G=	NP_001333369.1:n.1526+1G=
ENST00000355832.9:c.1526+1G=	ENSP00000348089.5:n.1526+1G=
ENST00000475116.1:n.116+1G=
ENST00000623073.3:c.-5260G=	ENSP00000485650.1:n.-5260G=
ENST00000623788.1:n.525+1G=
ENST00000679811.1:n.1610G=
ENST00000681632.1:n.1604+1G=
ENST00000681659.1:c.1526+1G=	ENSP00000505631.1:n.1526+1G=