Canonical Allele Identifier: CA2609135122

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49493058-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493058A>C , CM000672.2:g.49493058A>C	GRCh38
NC_000010.10:g.50701104A>C , CM000672.1:g.50701104A>C	GRCh37
NC_000010.9:g.50371110A>C	NCBI36
NG_009442.1:g.51044T>G , LRG_465:g.51044T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1821+59T>G MANE Select	ENSP00000348089.5:n.1821+59T>G
ENST00000681632.1:n.1899+59T>G
ENST00000681659.1:c.1662+59T>G	ENSP00000505631.1:n.1662+59T>G
ENST00000355832.9:c.1821+59T>G	ENSP00000348089.5:n.1821+59T>G
ENST00000475116.1:n.275+7480T>G
ENST00000623073.3:c.222+59T>G	ENSP00000485650.1:n.222+59T>G
ENST00000623115.3:c.-70+7480T>G	ENSP00000485321.1:n.-70+7480T>G
ENST00000623318.1:c.222+59T>G	ENSP00000485423.1:n.222+59T>G
NM_000124.3:c.1821+59T>G	NP_000115.1:n.1821+59T>G
NM_001346440.1:c.1821+59T>G	NP_001333369.1:n.1821+59T>G
NM_000124.4:c.1821+59T>G MANE Select	NP_000115.1:n.1821+59T>G
NM_001346440.2:c.1821+59T>G	NP_001333369.1:n.1821+59T>G