Canonical Allele Identifier: CA469790463

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732567C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524521C>G , CM000672.2:g.49524521C>G	GRCh38
NC_000010.10:g.50732567C>G , CM000672.1:g.50732567C>G	GRCh37
NC_000010.9:g.50402573C>G	NCBI36
NG_009442.1:g.19581G>C , LRG_465:g.19581G>C
NG_033155.1:g.4761G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.909G>C MANE Select	ENSP00000348089.5:p.Thr303=
ENST00000447839.7:c.909G>C MANE Plus Clinical	ENSP00000387966.2:p.Thr303=
ENST00000679596.1:c.*538G>C	ENSP00000504862.1:n.*538G>C
ENST00000679811.1:n.992G>C
ENST00000680107.1:c.652+3896G>C	ENSP00000505909.1:n.652+3896G>C
ENST00000680233.1:n.1002G>C
ENST00000681632.1:n.987G>C
ENST00000681659.1:c.909G>C	ENSP00000505631.1:p.Thr303=
ENST00000355832.9:c.909G>C	ENSP00000348089.5:p.Thr303=
ENST00000447839.6:c.909G>C	ENSP00000387966.2:p.Thr303=
ENST00000515869.1:c.909G>C	ENSP00000423550.1:p.Thr303=
NM_000124.3:c.909G>C	NP_000115.1:p.Thr303=
NM_001277058.1:c.909G>C	NP_001263987.1:p.Thr303=
NM_001277059.1:c.909G>C	NP_001263988.1:p.Thr303=
NM_001346440.1:c.909G>C	NP_001333369.1:p.Thr303=
NM_000124.4:c.909G>C MANE Select	NP_000115.1:p.Thr303=
NM_001277058.2:c.909G>C MANE Plus Clinical	NP_001263987.1:p.Thr303=
NM_001277059.2:c.909G>C	NP_001263988.1:p.Thr303=
NM_001346440.2:c.909G>C	NP_001333369.1:p.Thr303=