Canonical Allele Identifier: CA1908759989

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482628T= , CM000672.2:g.49482628T=	GRCh38
NC_000010.10:g.50690674T= , CM000672.1:g.50690674T=	GRCh37
NC_000010.9:g.50360680T=	NCBI36
NG_009442.1:g.61474A= , LRG_465:g.61474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2169+59A= MANE Select	ENSP00000348089.5:n.2169+59A=
ENST00000681632.1:n.2247+59A=
ENST00000681659.1:c.2010+59A=	ENSP00000505631.1:n.2010+59A=
ENST00000355832.9:c.2169+59A=	ENSP00000348089.5:n.2169+59A=
ENST00000623073.3:c.*561+59A=	ENSP00000485650.1:n.*561+59A=
ENST00000623115.3:c.279+59A=	ENSP00000485321.1:n.279+59A=
NM_000124.3:c.2169+59A=	NP_000115.1:n.2169+59A=
NM_001346440.1:c.2169+59A=	NP_001333369.1:n.2169+59A=
NM_000124.4:c.2169+59A= MANE Select	NP_000115.1:n.2169+59A=
NM_001346440.2:c.2169+59A=	NP_001333369.1:n.2169+59A=