Canonical Allele Identifier: CA1908749531

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470709G= , CM000672.2:g.49470709G=	GRCh38
NC_000010.10:g.50678755G= , CM000672.1:g.50678755G=	GRCh37
NC_000010.9:g.50348761G=	NCBI36
NG_009442.1:g.73393C= , LRG_465:g.73393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3251C= MANE Select	ENSP00000348089.5:p.Thr1084=
ENST00000679552.1:n.322C=
ENST00000679871.1:n.397C=
ENST00000679974.1:n.300C=
ENST00000681632.1:n.4654C=
ENST00000681659.1:c.3092C=	ENSP00000505631.1:p.Thr1031=
ENST00000355832.9:c.3251C=	ENSP00000348089.5:p.Thr1084=
ENST00000623073.3:c.*1547C=	ENSP00000485650.1:n.*1547C=
ENST00000623115.3:c.1361C=	ENSP00000485321.1:p.Thr454=
ENST00000624341.3:c.1083C=
NM_000124.3:c.3251C=	NP_000115.1:p.Thr1084=
XR_945953.1:n.243-856G=
NM_001346440.1:c.3251C=	NP_001333369.1:p.Thr1084=
NM_000124.4:c.3251C= MANE Select	NP_000115.1:p.Thr1084=
NM_001346440.2:c.3251C=	NP_001333369.1:p.Thr1084=