Canonical Allele Identifier: CA1908749418

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470458A= , CM000672.2:g.49470458A=	GRCh38
NC_000010.10:g.50678504A= , CM000672.1:g.50678504A=	GRCh37
NC_000010.9:g.50348510A=	NCBI36
NG_009442.1:g.73644T= , LRG_465:g.73644T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3502T= MANE Select	ENSP00000348089.5:p.Phe1168=
ENST00000679552.1:n.573T=
ENST00000679871.1:n.648T=
ENST00000679974.1:n.551T=
ENST00000681632.1:n.4905T=
ENST00000681659.1:c.3343T=	ENSP00000505631.1:p.Phe1115=
ENST00000355832.9:c.3502T=	ENSP00000348089.5:p.Phe1168=
ENST00000623073.3:c.*1798T=	ENSP00000485650.1:n.*1798T=
ENST00000623115.3:c.1612T=	ENSP00000485321.1:p.Phe538=
ENST00000624341.3:c.1334T=
NM_000124.3:c.3502T=	NP_000115.1:p.Phe1168=
XR_945953.1:n.243-1107A=
NM_001346440.1:c.3502T=	NP_001333369.1:p.Phe1168=
NM_000124.4:c.3502T= MANE Select	NP_000115.1:p.Phe1168=
NM_001346440.2:c.3502T=	NP_001333369.1:p.Phe1168=