Canonical Allele Identifier: CA376714009

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678471A>C (hg19) ; chr10:g.49470425A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470425A>C , CM000672.2:g.49470425A>C	GRCh38
NC_000010.10:g.50678471A>C , CM000672.1:g.50678471A>C	GRCh37
NC_000010.9:g.50348477A>C	NCBI36
NG_009442.1:g.73677T>G , LRG_465:g.73677T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3535T>G MANE Select	ENSP00000348089.5:p.Tyr1179Asp
ENST00000679552.1:n.606T>G
ENST00000679871.1:n.681T>G
ENST00000679974.1:n.584T>G
ENST00000681632.1:n.4938T>G
ENST00000681659.1:c.3376T>G	ENSP00000505631.1:p.Tyr1126Asp
ENST00000355832.9:c.3535T>G	ENSP00000348089.5:p.Tyr1179Asp
ENST00000623073.3:c.*1831T>G	ENSP00000485650.1:n.*1831T>G
ENST00000623115.3:c.1645T>G	ENSP00000485321.1:p.Tyr549Asp
ENST00000624341.3:c.1367T>G
NM_000124.3:c.3535T>G	NP_000115.1:p.Tyr1179Asp
XR_945953.1:n.243-1140A>C
NM_001346440.1:c.3535T>G	NP_001333369.1:p.Tyr1179Asp
NM_000124.4:c.3535T>G MANE Select	NP_000115.1:p.Tyr1179Asp
NM_001346440.2:c.3535T>G	NP_001333369.1:p.Tyr1179Asp