Canonical Allele Identifier: CA2609135272

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49493099-ACTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493100_49493102del , CM000672.2:g.49493100_49493102del	GRCh38
NC_000010.10:g.50701146_50701148del , CM000672.1:g.50701146_50701148del	GRCh37
NC_000010.9:g.50371152_50371154del	NCBI36
NG_009442.1:g.51000_51002del , LRG_465:g.51000_51002del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1821+15_1821+17del MANE Select	ENSP00000348089.5:n.1821+15_1821+17del
ENST00000681632.1:n.1899+15_1899+17del
ENST00000681659.1:c.1662+15_1662+17del	ENSP00000505631.1:n.1662+15_1662+17del
ENST00000355832.9:c.1821+15_1821+17del	ENSP00000348089.5:n.1821+15_1821+17del
ENST00000475116.1:n.275+7436_275+7438del
ENST00000623073.3:c.222+15_222+17del	ENSP00000485650.1:n.222+15_222+17del
ENST00000623115.3:c.-70+7436_-70+7438del	ENSP00000485321.1:n.-70+7436_-70+7438del
ENST00000623318.1:c.222+15_222+17del	ENSP00000485423.1:n.222+15_222+17del
NM_000124.3:c.1821+15_1821+17del	NP_000115.1:n.1821+15_1821+17del
NM_001346440.1:c.1821+15_1821+17del	NP_001333369.1:n.1821+15_1821+17del
NM_000124.4:c.1821+15_1821+17del MANE Select	NP_000115.1:n.1821+15_1821+17del
NM_001346440.2:c.1821+15_1821+17del	NP_001333369.1:n.1821+15_1821+17del