Canonical Allele Identifier: CA1908745580

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461629G= , CM000672.2:g.49461629G=	GRCh38
NC_000010.10:g.50669675G= , CM000672.1:g.50669675G=	GRCh37
NC_000010.9:g.50339681G=	NCBI36
NG_009442.1:g.82473C= , LRG_465:g.82473C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3779-73C= MANE Select	ENSP00000348089.5:n.3779-73C=
ENST00000679552.1:n.850-73C=
ENST00000679871.1:n.925-73C=
ENST00000679974.1:n.828-73C=
ENST00000681632.1:n.5182-73C=
ENST00000681659.1:c.3620-73C=	ENSP00000505631.1:n.3620-73C=
ENST00000355832.9:c.3779-73C=	ENSP00000348089.5:n.3779-73C=
ENST00000465653.1:n.101-73C=
ENST00000623073.3:c.*2075-73C=	ENSP00000485650.1:n.*2075-73C=
ENST00000623115.3:c.1889-73C=	ENSP00000485321.1:n.1889-73C=
ENST00000624341.3:c.1611-73C=
NM_000124.3:c.3779-73C=	NP_000115.1:n.3779-73C=
XR_945953.1:n.243-9936G=
NM_001346440.1:c.3779-73C=	NP_001333369.1:n.3779-73C=
NM_000124.4:c.3779-73C= MANE Select	NP_000115.1:n.3779-73C=
NM_001346440.2:c.3779-73C=	NP_001333369.1:n.3779-73C=