Canonical Allele Identifier: CA2609136083

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49500509-AGACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500513_49500516del , CM000672.2:g.49500513_49500516del	GRCh38
NC_000010.10:g.50708559_50708562del , CM000672.1:g.50708559_50708562del	GRCh37
NC_000010.9:g.50378565_50378568del	NCBI36
NG_009442.1:g.43589_43592del , LRG_465:g.43589_43592del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1685+25_1685+28del MANE Select	ENSP00000348089.5:n.1685+25_1685+28del
ENST00000681632.1:n.1763+25_1763+28del
ENST00000681659.1:c.1526+5371_1526+5374del	ENSP00000505631.1:n.1526+5371_1526+5374del
ENST00000355832.9:c.1685+25_1685+28del	ENSP00000348089.5:n.1685+25_1685+28del
ENST00000475116.1:n.275+25_275+28del
ENST00000623073.3:c.86+25_86+28del	ENSP00000485650.1:n.86+25_86+28del
ENST00000623115.3:c.-70+25_-70+28del	ENSP00000485321.1:n.-70+25_-70+28del
ENST00000623318.1:c.86+25_86+28del	ENSP00000485423.1:n.86+25_86+28del
NM_000124.3:c.1685+25_1685+28del	NP_000115.1:n.1685+25_1685+28del
NM_001346440.1:c.1685+25_1685+28del	NP_001333369.1:n.1685+25_1685+28del
NM_000124.4:c.1685+25_1685+28del MANE Select	NP_000115.1:n.1685+25_1685+28del
NM_001346440.2:c.1685+25_1685+28del	NP_001333369.1:n.1685+25_1685+28del