Canonical Allele Identifier: CA376714376

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470472-G-A
• MyVariant Identifiers: chr10:g.50678518G>A (hg19) ; chr10:g.49470472G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470472G>A , CM000672.2:g.49470472G>A	GRCh38
NC_000010.10:g.50678518G>A , CM000672.1:g.50678518G>A	GRCh37
NC_000010.9:g.50348524G>A	NCBI36
NG_009442.1:g.73630C>T , LRG_465:g.73630C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3488C>T MANE Select	ENSP00000348089.5:p.Ala1163Val
ENST00000679552.1:n.559C>T
ENST00000679871.1:n.634C>T
ENST00000679974.1:n.537C>T
ENST00000681632.1:n.4891C>T
ENST00000681659.1:c.3329C>T	ENSP00000505631.1:p.Ala1110Val
ENST00000355832.9:c.3488C>T	ENSP00000348089.5:p.Ala1163Val
ENST00000623073.3:c.*1784C>T	ENSP00000485650.1:n.*1784C>T
ENST00000623115.3:c.1598C>T	ENSP00000485321.1:p.Ala533Val
ENST00000624341.3:c.1320C>T
NM_000124.3:c.3488C>T	NP_000115.1:p.Ala1163Val
XR_945953.1:n.243-1093G>A
NM_001346440.1:c.3488C>T	NP_001333369.1:p.Ala1163Val
NM_000124.4:c.3488C>T MANE Select	NP_000115.1:p.Ala1163Val
NM_001346440.2:c.3488C>T	NP_001333369.1:p.Ala1163Val