Canonical Allele Identifier: CA376714032

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470427-A-G
• MyVariant Identifiers: chr10:g.50678473A>G (hg19) ; chr10:g.49470427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470427A>G , CM000672.2:g.49470427A>G	GRCh38
NC_000010.10:g.50678473A>G , CM000672.1:g.50678473A>G	GRCh37
NC_000010.9:g.50348479A>G	NCBI36
NG_009442.1:g.73675T>C , LRG_465:g.73675T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3533T>C MANE Select	ENSP00000348089.5:p.Phe1178Ser
ENST00000679552.1:n.604T>C
ENST00000679871.1:n.679T>C
ENST00000679974.1:n.582T>C
ENST00000681632.1:n.4936T>C
ENST00000681659.1:c.3374T>C	ENSP00000505631.1:p.Phe1125Ser
ENST00000355832.9:c.3533T>C	ENSP00000348089.5:p.Phe1178Ser
ENST00000623073.3:c.*1829T>C	ENSP00000485650.1:n.*1829T>C
ENST00000623115.3:c.1643T>C	ENSP00000485321.1:p.Phe548Ser
ENST00000624341.3:c.1365T>C
NM_000124.3:c.3533T>C	NP_000115.1:p.Phe1178Ser
XR_945953.1:n.243-1138A>G
NM_001346440.1:c.3533T>C	NP_001333369.1:p.Phe1178Ser
NM_000124.4:c.3533T>C MANE Select	NP_000115.1:p.Phe1178Ser
NM_001346440.2:c.3533T>C	NP_001333369.1:p.Phe1178Ser