Canonical Allele Identifier: CA1908749672

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470999T= , CM000672.2:g.49470999T=	GRCh38
NC_000010.10:g.50679045T= , CM000672.1:g.50679045T=	GRCh37
NC_000010.9:g.50349051T=	NCBI36
NG_009442.1:g.73103A= , LRG_465:g.73103A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3046A= MANE Select	ENSP00000348089.5:p.Thr1016=
ENST00000679552.1:n.142-110A=
ENST00000679871.1:n.192A=
ENST00000679974.1:n.120-110A=
ENST00000681632.1:n.4449A=
ENST00000681659.1:c.2887A=	ENSP00000505631.1:p.Thr963=
ENST00000355832.9:c.3046A=	ENSP00000348089.5:p.Thr1016=
ENST00000623073.3:c.*1342A=	ENSP00000485650.1:n.*1342A=
ENST00000623115.3:c.1156A=	ENSP00000485321.1:p.Thr386=
ENST00000624341.3:c.878A=
NM_000124.3:c.3046A=	NP_000115.1:p.Thr1016=
XR_945953.1:n.243-566T=
NM_001346440.1:c.3046A=	NP_001333369.1:p.Thr1016=
NM_000124.4:c.3046A= MANE Select	NP_000115.1:p.Thr1016=
NM_001346440.2:c.3046A=	NP_001333369.1:p.Thr1016=