Canonical Allele Identifier: CA1908749746

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471162C= , CM000672.2:g.49471162C=	GRCh38
NC_000010.10:g.50679208C= , CM000672.1:g.50679208C=	GRCh37
NC_000010.9:g.50349214C=	NCBI36
NG_009442.1:g.72940G= , LRG_465:g.72940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2925-42G= MANE Select	ENSP00000348089.5:n.2925-42G=
ENST00000679552.1:n.142-273G=
ENST00000679871.1:n.71-42G=
ENST00000679974.1:n.120-273G=
ENST00000681632.1:n.4328-42G=
ENST00000681659.1:c.2766-42G=	ENSP00000505631.1:n.2766-42G=
ENST00000355832.9:c.2925-42G=	ENSP00000348089.5:n.2925-42G=
ENST00000623073.3:c.*1221-42G=	ENSP00000485650.1:n.*1221-42G=
ENST00000623115.3:c.1035-42G=	ENSP00000485321.1:n.1035-42G=
ENST00000624341.3:c.757-42G=
NM_000124.3:c.2925-42G=	NP_000115.1:n.2925-42G=
XR_945953.1:n.243-403C=
NM_001346440.1:c.2925-42G=	NP_001333369.1:n.2925-42G=
NM_000124.4:c.2925-42G= MANE Select	NP_000115.1:n.2925-42G=
NM_001346440.2:c.2925-42G=	NP_001333369.1:n.2925-42G=