Canonical Allele Identifier: CA1908745525

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461509T= , CM000672.2:g.49461509T=	GRCh38
NC_000010.10:g.50669555T= , CM000672.1:g.50669555T=	GRCh37
NC_000010.9:g.50339561T=	NCBI36
NG_009442.1:g.82593A= , LRG_465:g.82593A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3826A= MANE Select	ENSP00000348089.5:p.Ser1276=
ENST00000679552.1:n.897A=
ENST00000679871.1:n.972A=
ENST00000679974.1:n.875A=
ENST00000681632.1:n.5229A=
ENST00000681659.1:c.3667A=	ENSP00000505631.1:p.Ser1223=
ENST00000355832.9:c.3826A=	ENSP00000348089.5:p.Ser1276=
ENST00000465653.1:n.148A=
ENST00000623073.3:c.*2122A=	ENSP00000485650.1:n.*2122A=
ENST00000623115.3:c.1936A=	ENSP00000485321.1:p.Ser646=
ENST00000624341.3:c.1658A=
NM_000124.3:c.3826A=	NP_000115.1:p.Ser1276=
XR_945953.1:n.243-10056T=
NM_001346440.1:c.3826A=	NP_001333369.1:p.Ser1276=
NM_000124.4:c.3826A= MANE Select	NP_000115.1:p.Ser1276=
NM_001346440.2:c.3826A=	NP_001333369.1:p.Ser1276=