Canonical Allele Identifier: CA2574544823

Gene: ERCC6

Linked Data

• dbSNP Id: rs2132526341

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461291T>C , CM000672.2:g.49461291T>C	GRCh38
NC_000010.10:g.50669337T>C , CM000672.1:g.50669337T>C	GRCh37
NC_000010.9:g.50339343T>C	NCBI36
NG_009442.1:g.82811A>G , LRG_465:g.82811A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3983+61A>G MANE Select	ENSP00000348089.5:n.3983+61A>G
ENST00000679552.1:n.1054+61A>G
ENST00000679871.1:n.1129+61A>G
ENST00000679974.1:n.1032+61A>G
ENST00000681632.1:n.5386+61A>G
ENST00000681659.1:c.3824+61A>G	ENSP00000505631.1:n.3824+61A>G
ENST00000355832.9:c.3983+61A>G	ENSP00000348089.5:n.3983+61A>G
ENST00000465653.1:n.305+61A>G
ENST00000623073.3:c.*2279+61A>G	ENSP00000485650.1:n.*2279+61A>G
ENST00000623115.3:c.2093+61A>G	ENSP00000485321.1:n.2093+61A>G
ENST00000624341.3:c.1815+61A>G
NM_000124.3:c.3983+61A>G	NP_000115.1:n.3983+61A>G
XR_945953.1:n.243-10274T>C
NM_001346440.1:c.3983+61A>G	NP_001333369.1:n.3983+61A>G
NM_000124.4:c.3983+61A>G MANE Select	NP_000115.1:n.3983+61A>G
NM_001346440.2:c.3983+61A>G	NP_001333369.1:n.3983+61A>G