Canonical Allele Identifier: CA5496434

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 2403755
• ClinVar RCV Id: RCV002754180
• dbSNP Id: rs528081368
• ExAC: 10:50732667 C / T
• gnomAD v2: 10-50732667-C-T
• gnomAD v3: 10-49524621-C-T
• gnomAD v4: 10-49524621-C-T
• MyVariant Identifiers: chr10:g.50732667C>T (hg19) ; chr10:g.49524621C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524621C>T , CM000672.2:g.49524621C>T	GRCh38
NC_000010.10:g.50732667C>T , CM000672.1:g.50732667C>T	GRCh37
NC_000010.9:g.50402673C>T	NCBI36
NG_009442.1:g.19481G>A , LRG_465:g.19481G>A
NG_033155.1:g.4661G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.809G>A MANE Select	ENSP00000348089.5:p.Gly270Asp
ENST00000447839.7:c.809G>A MANE Plus Clinical	ENSP00000387966.2:p.Gly270Asp
ENST00000679596.1:c.*438G>A	ENSP00000504862.1:n.*438G>A
ENST00000679811.1:n.892G>A
ENST00000680107.1:c.652+3796G>A	ENSP00000505909.1:n.652+3796G>A
ENST00000680233.1:n.902G>A
ENST00000681632.1:n.887G>A
ENST00000681659.1:c.809G>A	ENSP00000505631.1:p.Gly270Asp
ENST00000355832.9:c.809G>A	ENSP00000348089.5:p.Gly270Asp
ENST00000447839.6:c.809G>A	ENSP00000387966.2:p.Gly270Asp
ENST00000515869.1:c.809G>A	ENSP00000423550.1:p.Gly270Asp
NM_000124.3:c.809G>A	NP_000115.1:p.Gly270Asp
NM_001277058.1:c.809G>A	NP_001263987.1:p.Gly270Asp
NM_001277059.1:c.809G>A	NP_001263988.1:p.Gly270Asp
NM_001346440.1:c.809G>A	NP_001333369.1:p.Gly270Asp
NM_000124.4:c.809G>A MANE Select	NP_000115.1:p.Gly270Asp
NM_001277058.2:c.809G>A MANE Plus Clinical	NP_001263987.1:p.Gly270Asp
NM_001277059.2:c.809G>A	NP_001263988.1:p.Gly270Asp
NM_001346440.2:c.809G>A	NP_001333369.1:p.Gly270Asp