Canonical Allele Identifier: CA1908745593

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461659G= , CM000672.2:g.49461659G=	GRCh38
NC_000010.10:g.50669705G= , CM000672.1:g.50669705G=	GRCh37
NC_000010.9:g.50339711G=	NCBI36
NG_009442.1:g.82443C= , LRG_465:g.82443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3779-103C= MANE Select	ENSP00000348089.5:n.3779-103C=
ENST00000679552.1:n.850-103C=
ENST00000679871.1:n.925-103C=
ENST00000679974.1:n.828-103C=
ENST00000681632.1:n.5182-103C=
ENST00000681659.1:c.3620-103C=	ENSP00000505631.1:n.3620-103C=
ENST00000355832.9:c.3779-103C=	ENSP00000348089.5:n.3779-103C=
ENST00000465653.1:n.101-103C=
ENST00000623073.3:c.*2075-103C=	ENSP00000485650.1:n.*2075-103C=
ENST00000623115.3:c.1889-103C=	ENSP00000485321.1:n.1889-103C=
ENST00000624341.3:c.1611-103C=
NM_000124.3:c.3779-103C=	NP_000115.1:n.3779-103C=
XR_945953.1:n.243-9906G=
NM_001346440.1:c.3779-103C=	NP_001333369.1:n.3779-103C=
NM_000124.4:c.3779-103C= MANE Select	NP_000115.1:n.3779-103C=
NM_001346440.2:c.3779-103C=	NP_001333369.1:n.3779-103C=