Canonical Allele Identifier: CA469600278

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49461378-C-T
• MyVariant Identifiers: chr10:g.50669424C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461378C>T , CM000672.2:g.49461378C>T	GRCh38
NC_000010.10:g.50669424C>T , CM000672.1:g.50669424C>T	GRCh37
NC_000010.9:g.50339430C>T	NCBI36
NG_009442.1:g.82724G>A , LRG_465:g.82724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3957G>A MANE Select	ENSP00000348089.5:p.Gly1319=
ENST00000679552.1:n.1028G>A
ENST00000679871.1:n.1103G>A
ENST00000679974.1:n.1006G>A
ENST00000681632.1:n.5360G>A
ENST00000681659.1:c.3798G>A	ENSP00000505631.1:p.Gly1266=
ENST00000355832.9:c.3957G>A	ENSP00000348089.5:p.Gly1319=
ENST00000465653.1:n.279G>A
ENST00000623073.3:c.*2253G>A	ENSP00000485650.1:n.*2253G>A
ENST00000623115.3:c.2067G>A	ENSP00000485321.1:p.Gly689=
ENST00000624341.3:c.1789G>A
NM_000124.3:c.3957G>A	NP_000115.1:p.Gly1319=
XR_945953.1:n.243-10187C>T
NM_001346440.1:c.3957G>A	NP_001333369.1:p.Gly1319=
NM_000124.4:c.3957G>A MANE Select	NP_000115.1:p.Gly1319=
NM_001346440.2:c.3957G>A	NP_001333369.1:p.Gly1319=