Canonical Allele Identifier: CA376716197

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678767A>G (hg19) ; chr10:g.49470721A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470721A>G , CM000672.2:g.49470721A>G	GRCh38
NC_000010.10:g.50678767A>G , CM000672.1:g.50678767A>G	GRCh37
NC_000010.9:g.50348773A>G	NCBI36
NG_009442.1:g.73381T>C , LRG_465:g.73381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3239T>C MANE Select	ENSP00000348089.5:p.Val1080Ala
ENST00000679552.1:n.310T>C
ENST00000679871.1:n.385T>C
ENST00000679974.1:n.288T>C
ENST00000681632.1:n.4642T>C
ENST00000681659.1:c.3080T>C	ENSP00000505631.1:p.Val1027Ala
ENST00000355832.9:c.3239T>C	ENSP00000348089.5:p.Val1080Ala
ENST00000623073.3:c.*1535T>C	ENSP00000485650.1:n.*1535T>C
ENST00000623115.3:c.1349T>C	ENSP00000485321.1:p.Val450Ala
ENST00000624341.3:c.1071T>C
NM_000124.3:c.3239T>C	NP_000115.1:p.Val1080Ala
XR_945953.1:n.243-844A>G
NM_001346440.1:c.3239T>C	NP_001333369.1:p.Val1080Ala
NM_000124.4:c.3239T>C MANE Select	NP_000115.1:p.Val1080Ala
NM_001346440.2:c.3239T>C	NP_001333369.1:p.Val1080Ala