Canonical Allele Identifier: CA1908745041

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49460345T= , CM000672.2:g.49460345T=	GRCh38
NC_000010.10:g.50668391T= , CM000672.1:g.50668391T=	GRCh37
NC_000010.9:g.50338397T=	NCBI36
NG_009442.1:g.83757A= , LRG_465:g.83757A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.4062+28A= MANE Select	ENSP00000348089.5:n.4062+28A=
ENST00000679552.1:n.1161A=
ENST00000679871.1:n.1208+28A=
ENST00000679974.1:n.1111+28A=
ENST00000681632.1:n.5465+28A=
ENST00000681659.1:c.3903+28A=	ENSP00000505631.1:n.3903+28A=
ENST00000355832.9:c.4062+28A=	ENSP00000348089.5:n.4062+28A=
ENST00000465653.1:n.412A=
ENST00000623073.3:c.*2358+28A=	ENSP00000485650.1:n.*2358+28A=
ENST00000623115.3:c.2172+28A=	ENSP00000485321.1:n.2172+28A=
ENST00000624341.3:c.1894+28A=
NM_000124.3:c.4062+28A=	NP_000115.1:n.4062+28A=
XR_945953.1:n.243-11220T=
NM_001346440.1:c.4062+28A=	NP_001333369.1:n.4062+28A=
NM_000124.4:c.4062+28A= MANE Select	NP_000115.1:n.4062+28A=
NM_001346440.2:c.4062+28A=	NP_001333369.1:n.4062+28A=