Canonical Allele Identifier: CA1908778556

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500698T= , CM000672.2:g.49500698T=	GRCh38
NC_000010.10:g.50708744T= , CM000672.1:g.50708744T=	GRCh37
NC_000010.9:g.50378750T=	NCBI36
NG_009442.1:g.43404A= , LRG_465:g.43404A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1527-2A= MANE Select	ENSP00000348089.5:n.1527-2A=
ENST00000681632.1:n.1605-2A=
ENST00000681659.1:c.1526+5186A=	ENSP00000505631.1:n.1526+5186A=
ENST00000355832.9:c.1527-2A=	ENSP00000348089.5:n.1527-2A=
ENST00000475116.1:n.117-2A=
ENST00000623073.3:c.-75A=	ENSP00000485650.1:n.-75A=
ENST00000623115.3:c.-228-2A=	ENSP00000485321.1:n.-228-2A=
ENST00000623318.1:c.-73-2A=	ENSP00000485423.1:n.-73-2A=
ENST00000623788.1:n.526-2A=
NM_000124.3:c.1527-2A=	NP_000115.1:n.1527-2A=
NM_001346440.1:c.1527-2A=	NP_001333369.1:n.1527-2A=
NM_000124.4:c.1527-2A= MANE Select	NP_000115.1:n.1527-2A=
NM_001346440.2:c.1527-2A=	NP_001333369.1:n.1527-2A=