Canonical Allele Identifier: CA376726482

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50701209A>G (hg19) ; chr10:g.49493163A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493163A>G , CM000672.2:g.49493163A>G	GRCh38
NC_000010.10:g.50701209A>G , CM000672.1:g.50701209A>G	GRCh37
NC_000010.9:g.50371215A>G	NCBI36
NG_009442.1:g.50939T>C , LRG_465:g.50939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1775T>C MANE Select	ENSP00000348089.5:p.Phe592Ser
ENST00000681632.1:n.1853T>C
ENST00000681659.1:c.1616T>C	ENSP00000505631.1:p.Phe539Ser
ENST00000355832.9:c.1775T>C	ENSP00000348089.5:p.Phe592Ser
ENST00000475116.1:n.275+7375T>C
ENST00000623073.3:c.176T>C	ENSP00000485650.1:p.Phe59Ser
ENST00000623115.3:c.-70+7375T>C	ENSP00000485321.1:n.-70+7375T>C
ENST00000623318.1:c.176T>C	ENSP00000485423.1:p.Phe59Ser
NM_000124.3:c.1775T>C	NP_000115.1:p.Phe592Ser
NM_001346440.1:c.1775T>C	NP_001333369.1:p.Phe592Ser
NM_000124.4:c.1775T>C MANE Select	NP_000115.1:p.Phe592Ser
NM_001346440.2:c.1775T>C	NP_001333369.1:p.Phe592Ser