Canonical Allele Identifier: CA1908752965

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49514720T= , CM000672.2:g.49514720T=	GRCh38
NC_000010.10:g.50722766T= , CM000672.1:g.50722766T=	GRCh37
NC_000010.9:g.50392772T=	NCBI36
NG_009442.1:g.29382A= , LRG_465:g.29382A=
NG_033155.1:g.14562A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1398-8708A= MANE Select	ENSP00000348089.5:n.1398-8708A=
ENST00000679811.1:n.1481-8708A=
ENST00000680107.1:c.*2379A=	ENSP00000505909.1:n.*2379A=
ENST00000681632.1:n.1476-8708A=
ENST00000681659.1:c.1398-8708A=	ENSP00000505631.1:n.1398-8708A=
ENST00000355832.9:c.1398-8708A=	ENSP00000348089.5:n.1398-8708A=
NM_000124.3:c.1398-8708A=	NP_000115.1:n.1398-8708A=
NM_001346440.1:c.1398-8708A=	NP_001333369.1:n.1398-8708A=
NM_000124.4:c.1398-8708A= MANE Select	NP_000115.1:n.1398-8708A=
NM_001346440.2:c.1398-8708A=	NP_001333369.1:n.1398-8708A=