Canonical Allele Identifier: CA376716435

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678807T>C (hg19) ; chr10:g.49470761T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470761T>C , CM000672.2:g.49470761T>C	GRCh38
NC_000010.10:g.50678807T>C , CM000672.1:g.50678807T>C	GRCh37
NC_000010.9:g.50348813T>C	NCBI36
NG_009442.1:g.73341A>G , LRG_465:g.73341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3199A>G MANE Select	ENSP00000348089.5:p.Thr1067Ala
ENST00000679552.1:n.270A>G
ENST00000679871.1:n.345A>G
ENST00000679974.1:n.248A>G
ENST00000681632.1:n.4602A>G
ENST00000681659.1:c.3040A>G	ENSP00000505631.1:p.Thr1014Ala
ENST00000355832.9:c.3199A>G	ENSP00000348089.5:p.Thr1067Ala
ENST00000623073.3:c.*1495A>G	ENSP00000485650.1:n.*1495A>G
ENST00000623115.3:c.1309A>G	ENSP00000485321.1:p.Thr437Ala
ENST00000624341.3:c.1031A>G
NM_000124.3:c.3199A>G	NP_000115.1:p.Thr1067Ala
XR_945953.1:n.243-804T>C
NM_001346440.1:c.3199A>G	NP_001333369.1:p.Thr1067Ala
NM_000124.4:c.3199A>G MANE Select	NP_000115.1:p.Thr1067Ala
NM_001346440.2:c.3199A>G	NP_001333369.1:p.Thr1067Ala