Canonical Allele Identifier: CA376716589

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470788-C-G
• MyVariant Identifiers: chr10:g.50678834C>G (hg19) ; chr10:g.49470788C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470788C>G , CM000672.2:g.49470788C>G	GRCh38
NC_000010.10:g.50678834C>G , CM000672.1:g.50678834C>G	GRCh37
NC_000010.9:g.50348840C>G	NCBI36
NG_009442.1:g.73314G>C , LRG_465:g.73314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3172G>C MANE Select	ENSP00000348089.5:p.Ala1058Pro
ENST00000679552.1:n.243G>C
ENST00000679871.1:n.318G>C
ENST00000679974.1:n.221G>C
ENST00000681632.1:n.4575G>C
ENST00000681659.1:c.3013G>C	ENSP00000505631.1:p.Ala1005Pro
ENST00000355832.9:c.3172G>C	ENSP00000348089.5:p.Ala1058Pro
ENST00000623073.3:c.*1468G>C	ENSP00000485650.1:n.*1468G>C
ENST00000623115.3:c.1282G>C	ENSP00000485321.1:p.Ala428Pro
ENST00000624341.3:c.1004G>C
NM_000124.3:c.3172G>C	NP_000115.1:p.Ala1058Pro
XR_945953.1:n.243-777C>G
NM_001346440.1:c.3172G>C	NP_001333369.1:p.Ala1058Pro
NM_000124.4:c.3172G>C MANE Select	NP_000115.1:p.Ala1058Pro
NM_001346440.2:c.3172G>C	NP_001333369.1:p.Ala1058Pro