Canonical Allele Identifier: CA376708608

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669560C>G (hg19) ; chr10:g.49461514C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461514C>G , CM000672.2:g.49461514C>G	GRCh38
NC_000010.10:g.50669560C>G , CM000672.1:g.50669560C>G	GRCh37
NC_000010.9:g.50339566C>G	NCBI36
NG_009442.1:g.82588G>C , LRG_465:g.82588G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3821G>C MANE Select	ENSP00000348089.5:p.Gly1274Ala
ENST00000679552.1:n.892G>C
ENST00000679871.1:n.967G>C
ENST00000679974.1:n.870G>C
ENST00000681632.1:n.5224G>C
ENST00000681659.1:c.3662G>C	ENSP00000505631.1:p.Gly1221Ala
ENST00000355832.9:c.3821G>C	ENSP00000348089.5:p.Gly1274Ala
ENST00000465653.1:n.143G>C
ENST00000623073.3:c.*2117G>C	ENSP00000485650.1:n.*2117G>C
ENST00000623115.3:c.1931G>C	ENSP00000485321.1:p.Gly644Ala
ENST00000624341.3:c.1653G>C
NM_000124.3:c.3821G>C	NP_000115.1:p.Gly1274Ala
XR_945953.1:n.243-10051C>G
NM_001346440.1:c.3821G>C	NP_001333369.1:p.Gly1274Ala
NM_000124.4:c.3821G>C MANE Select	NP_000115.1:p.Gly1274Ala
NM_001346440.2:c.3821G>C	NP_001333369.1:p.Gly1274Ala