Canonical Allele Identifier: CA2609136073

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49500502-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500502G>A , CM000672.2:g.49500502G>A	GRCh38
NC_000010.10:g.50708548G>A , CM000672.1:g.50708548G>A	GRCh37
NC_000010.9:g.50378554G>A	NCBI36
NG_009442.1:g.43600C>T , LRG_465:g.43600C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1685+36C>T MANE Select	ENSP00000348089.5:n.1685+36C>T
ENST00000681632.1:n.1763+36C>T
ENST00000681659.1:c.1526+5382C>T	ENSP00000505631.1:n.1526+5382C>T
ENST00000355832.9:c.1685+36C>T	ENSP00000348089.5:n.1685+36C>T
ENST00000475116.1:n.275+36C>T
ENST00000623073.3:c.86+36C>T	ENSP00000485650.1:n.86+36C>T
ENST00000623115.3:c.-70+36C>T	ENSP00000485321.1:n.-70+36C>T
ENST00000623318.1:c.86+36C>T	ENSP00000485423.1:n.86+36C>T
NM_000124.3:c.1685+36C>T	NP_000115.1:n.1685+36C>T
NM_001346440.1:c.1685+36C>T	NP_001333369.1:n.1685+36C>T
NM_000124.4:c.1685+36C>T MANE Select	NP_000115.1:n.1685+36C>T
NM_001346440.2:c.1685+36C>T	NP_001333369.1:n.1685+36C>T