Canonical Allele Identifier: CA1908745507

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461466G= , CM000672.2:g.49461466G=	GRCh38
NC_000010.10:g.50669512G= , CM000672.1:g.50669512G=	GRCh37
NC_000010.9:g.50339518G=	NCBI36
NG_009442.1:g.82636C= , LRG_465:g.82636C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3869C= MANE Select	ENSP00000348089.5:p.Ala1290=
ENST00000679552.1:n.940C=
ENST00000679871.1:n.1015C=
ENST00000679974.1:n.918C=
ENST00000681632.1:n.5272C=
ENST00000681659.1:c.3710C=	ENSP00000505631.1:p.Ala1237=
ENST00000355832.9:c.3869C=	ENSP00000348089.5:p.Ala1290=
ENST00000465653.1:n.191C=
ENST00000623073.3:c.*2165C=	ENSP00000485650.1:n.*2165C=
ENST00000623115.3:c.1979C=	ENSP00000485321.1:p.Ala660=
ENST00000624341.3:c.1701C=
NM_000124.3:c.3869C=	NP_000115.1:p.Ala1290=
XR_945953.1:n.243-10099G=
NM_001346440.1:c.3869C=	NP_001333369.1:p.Ala1290=
NM_000124.4:c.3869C= MANE Select	NP_000115.1:p.Ala1290=
NM_001346440.2:c.3869C=	NP_001333369.1:p.Ala1290=