Canonical Allele Identifier: CA376704879

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50667282T>A (hg19) ; chr10:g.49459236T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49459236T>A , CM000672.2:g.49459236T>A	GRCh38
NC_000010.10:g.50667282T>A , CM000672.1:g.50667282T>A	GRCh37
NC_000010.9:g.50337288T>A	NCBI36
NG_009442.1:g.84866A>T , LRG_465:g.84866A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.4063-2A>T MANE Select	ENSP00000348089.5:n.4063-2A>T
ENST00000679552.1:n.2270A>T
ENST00000679871.1:n.1209-2A>T
ENST00000679974.1:n.1112-2A>T
ENST00000681632.1:n.5466-2A>T
ENST00000681659.1:c.3904-2A>T	ENSP00000505631.1:n.3904-2A>T
ENST00000355832.9:c.4063-2A>T	ENSP00000348089.5:n.4063-2A>T
ENST00000623073.3:c.*2359-2A>T	ENSP00000485650.1:n.*2359-2A>T
ENST00000623115.3:c.2173-2A>T	ENSP00000485321.1:n.2173-2A>T
ENST00000624341.3:c.1895-2A>T
NM_000124.3:c.4063-2A>T	NP_000115.1:n.4063-2A>T
XR_945953.1:n.243-12329T>A
NM_001346440.1:c.4063-2A>T	NP_001333369.1:n.4063-2A>T
NM_000124.4:c.4063-2A>T MANE Select	NP_000115.1:n.4063-2A>T
NM_001346440.2:c.4063-2A>T	NP_001333369.1:n.4063-2A>T