Canonical Allele Identifier: CA469604014

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50690799A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482753A>T , CM000672.2:g.49482753A>T	GRCh38
NC_000010.10:g.50690799A>T , CM000672.1:g.50690799A>T	GRCh37
NC_000010.9:g.50360805A>T	NCBI36
NG_009442.1:g.61349T>A , LRG_465:g.61349T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2103T>A MANE Select	ENSP00000348089.5:p.Pro701=
ENST00000681632.1:n.2181T>A
ENST00000681659.1:c.1944T>A	ENSP00000505631.1:p.Pro648=
ENST00000355832.9:c.2103T>A	ENSP00000348089.5:p.Pro701=
ENST00000623073.3:c.*495T>A	ENSP00000485650.1:n.*495T>A
ENST00000623115.3:c.213T>A	ENSP00000485321.1:p.Pro71=
NM_000124.3:c.2103T>A	NP_000115.1:p.Pro701=
NM_001346440.1:c.2103T>A	NP_001333369.1:p.Pro701=
NM_000124.4:c.2103T>A MANE Select	NP_000115.1:p.Pro701=
NM_001346440.2:c.2103T>A	NP_001333369.1:p.Pro701=