Canonical Allele Identifier: CA1908772069

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49492879C= , CM000672.2:g.49492879C=	GRCh38
NC_000010.10:g.50700925C= , CM000672.1:g.50700925C=	GRCh37
NC_000010.9:g.50370931C=	NCBI36
NG_009442.1:g.51223G= , LRG_465:g.51223G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1821+238G= MANE Select	ENSP00000348089.5:n.1821+238G=
ENST00000681632.1:n.1899+238G=
ENST00000681659.1:c.1662+238G=	ENSP00000505631.1:n.1662+238G=
ENST00000355832.9:c.1821+238G=	ENSP00000348089.5:n.1821+238G=
ENST00000475116.1:n.275+7659G=
ENST00000623073.3:c.222+238G=	ENSP00000485650.1:n.222+238G=
ENST00000623115.3:c.-70+7659G=	ENSP00000485321.1:n.-70+7659G=
ENST00000623318.1:c.222+238G=	ENSP00000485423.1:n.222+238G=
NM_000124.3:c.1821+238G=	NP_000115.1:n.1821+238G=
NM_001346440.1:c.1821+238G=	NP_001333369.1:n.1821+238G=
NM_000124.4:c.1821+238G= MANE Select	NP_000115.1:n.1821+238G=
NM_001346440.2:c.1821+238G=	NP_001333369.1:n.1821+238G=