Canonical Allele Identifier: CA2787930235

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493283_49493297del , CM000672.2:g.49493283_49493297del	GRCh38
NC_000010.10:g.50701329_50701343del , CM000672.1:g.50701329_50701343del	GRCh37
NC_000010.9:g.50371335_50371349del	NCBI36
NG_009442.1:g.50805_50819del , LRG_465:g.50805_50819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1686-45_1686-31del MANE Select	ENSP00000348089.5:n.1686-45_1686-31del
ENST00000681632.1:n.1764-45_1764-31del
ENST00000681659.1:c.1527-45_1527-31del	ENSP00000505631.1:n.1527-45_1527-31del
ENST00000355832.9:c.1686-45_1686-31del	ENSP00000348089.5:n.1686-45_1686-31del
ENST00000475116.1:n.275+7241_275+7255del
ENST00000623073.3:c.87-45_87-31del	ENSP00000485650.1:n.87-45_87-31del
ENST00000623115.3:c.-70+7241_-70+7255del	ENSP00000485321.1:n.-70+7241_-70+7255del
ENST00000623318.1:c.87-45_87-31del	ENSP00000485423.1:n.87-45_87-31del
NM_000124.3:c.1686-45_1686-31del	NP_000115.1:n.1686-45_1686-31del
NM_001346440.1:c.1686-45_1686-31del	NP_001333369.1:n.1686-45_1686-31del
NM_000124.4:c.1686-45_1686-31del MANE Select	NP_000115.1:n.1686-45_1686-31del
NM_001346440.2:c.1686-45_1686-31del	NP_001333369.1:n.1686-45_1686-31del