Canonical Allele Identifier: CA1908749580

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470817T= , CM000672.2:g.49470817T=	GRCh38
NC_000010.10:g.50678863T= , CM000672.1:g.50678863T=	GRCh37
NC_000010.9:g.50348869T=	NCBI36
NG_009442.1:g.73285A= , LRG_465:g.73285A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3143A= MANE Select	ENSP00000348089.5:p.His1048=
ENST00000679552.1:n.214A=
ENST00000679871.1:n.289A=
ENST00000679974.1:n.192A=
ENST00000681632.1:n.4546A=
ENST00000681659.1:c.2984A=	ENSP00000505631.1:p.His995=
ENST00000355832.9:c.3143A=	ENSP00000348089.5:p.His1048=
ENST00000623073.3:c.*1439A=	ENSP00000485650.1:n.*1439A=
ENST00000623115.3:c.1253A=	ENSP00000485321.1:p.His418=
ENST00000624341.3:c.975A=
NM_000124.3:c.3143A=	NP_000115.1:p.His1048=
XR_945953.1:n.243-748T=
NM_001346440.1:c.3143A=	NP_001333369.1:p.His1048=
NM_000124.4:c.3143A= MANE Select	NP_000115.1:p.His1048=
NM_001346440.2:c.3143A=	NP_001333369.1:p.His1048=