Canonical Allele Identifier: CA2609135788

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49493352-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493359dup , CM000672.2:g.49493359dup	GRCh38
NC_000010.10:g.50701405dup , CM000672.1:g.50701405dup	GRCh37
NC_000010.9:g.50371411dup	NCBI36
NG_009442.1:g.50749dup , LRG_465:g.50749dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1686-101dup MANE Select	ENSP00000348089.5:n.1686-101dup
ENST00000681632.1:n.1764-101dup
ENST00000681659.1:c.1527-101dup	ENSP00000505631.1:n.1527-101dup
ENST00000355832.9:c.1686-101dup	ENSP00000348089.5:n.1686-101dup
ENST00000475116.1:n.275+7185dup
ENST00000623073.3:c.87-101dup	ENSP00000485650.1:n.87-101dup
ENST00000623115.3:c.-70+7185dup	ENSP00000485321.1:n.-70+7185dup
ENST00000623318.1:c.87-101dup	ENSP00000485423.1:n.87-101dup
NM_000124.3:c.1686-101dup	NP_000115.1:n.1686-101dup
NM_001346440.1:c.1686-101dup	NP_001333369.1:n.1686-101dup
NM_000124.4:c.1686-101dup MANE Select	NP_000115.1:n.1686-101dup
NM_001346440.2:c.1686-101dup	NP_001333369.1:n.1686-101dup