Canonical Allele Identifier: CA1908752995

Gene: ERCC6

Linked Data

• dbSNP Id: rs1836898786

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49514795del , CM000672.2:g.49514795del	GRCh38
NC_000010.10:g.50722841del , CM000672.1:g.50722841del	GRCh37
NC_000010.9:g.50392847del	NCBI36
NG_009442.1:g.29307del , LRG_465:g.29307del
NG_033155.1:g.14487del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1398-8783del MANE Select	ENSP00000348089.5:n.1398-8783del
ENST00000679811.1:n.1481-8783del
ENST00000680107.1:c.*2304del	ENSP00000505909.1:n.*2304del
ENST00000681632.1:n.1476-8783del
ENST00000681659.1:c.1398-8783del	ENSP00000505631.1:n.1398-8783del
ENST00000355832.9:c.1398-8783del	ENSP00000348089.5:n.1398-8783del
NM_000124.3:c.1398-8783del	NP_000115.1:n.1398-8783del
NM_001346440.1:c.1398-8783del	NP_001333369.1:n.1398-8783del
NM_000124.4:c.1398-8783del MANE Select	NP_000115.1:n.1398-8783del
NM_001346440.2:c.1398-8783del	NP_001333369.1:n.1398-8783del