Canonical Allele Identifier: CA469790482

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732582A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524536A>G , CM000672.2:g.49524536A>G	GRCh38
NC_000010.10:g.50732582A>G , CM000672.1:g.50732582A>G	GRCh37
NC_000010.9:g.50402588A>G	NCBI36
NG_009442.1:g.19566T>C , LRG_465:g.19566T>C
NG_033155.1:g.4746T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.894T>C MANE Select	ENSP00000348089.5:p.Ala298=
ENST00000447839.7:c.894T>C MANE Plus Clinical	ENSP00000387966.2:p.Ala298=
ENST00000679596.1:c.*523T>C	ENSP00000504862.1:n.*523T>C
ENST00000679811.1:n.977T>C
ENST00000680107.1:c.652+3881T>C	ENSP00000505909.1:n.652+3881T>C
ENST00000680233.1:n.987T>C
ENST00000681632.1:n.972T>C
ENST00000681659.1:c.894T>C	ENSP00000505631.1:p.Ala298=
ENST00000355832.9:c.894T>C	ENSP00000348089.5:p.Ala298=
ENST00000447839.6:c.894T>C	ENSP00000387966.2:p.Ala298=
ENST00000515869.1:c.894T>C	ENSP00000423550.1:p.Ala298=
NM_000124.3:c.894T>C	NP_000115.1:p.Ala298=
NM_001277058.1:c.894T>C	NP_001263987.1:p.Ala298=
NM_001277059.1:c.894T>C	NP_001263988.1:p.Ala298=
NM_001346440.1:c.894T>C	NP_001333369.1:p.Ala298=
NM_000124.4:c.894T>C MANE Select	NP_000115.1:p.Ala298=
NM_001277058.2:c.894T>C MANE Plus Clinical	NP_001263987.1:p.Ala298=
NM_001277059.2:c.894T>C	NP_001263988.1:p.Ala298=
NM_001346440.2:c.894T>C	NP_001333369.1:p.Ala298=