Canonical Allele Identifier: CA1908745403

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461263A= , CM000672.2:g.49461263A=	GRCh38
NC_000010.10:g.50669309A= , CM000672.1:g.50669309A=	GRCh37
NC_000010.9:g.50339315A=	NCBI36
NG_009442.1:g.82839T= , LRG_465:g.82839T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3983+89T= MANE Select	ENSP00000348089.5:n.3983+89T=
ENST00000679552.1:n.1054+89T=
ENST00000679871.1:n.1129+89T=
ENST00000679974.1:n.1032+89T=
ENST00000681632.1:n.5386+89T=
ENST00000681659.1:c.3824+89T=	ENSP00000505631.1:n.3824+89T=
ENST00000355832.9:c.3983+89T=	ENSP00000348089.5:n.3983+89T=
ENST00000465653.1:n.305+89T=
ENST00000623073.3:c.*2279+89T=	ENSP00000485650.1:n.*2279+89T=
ENST00000623115.3:c.2093+89T=	ENSP00000485321.1:n.2093+89T=
ENST00000624341.3:c.1815+89T=
NM_000124.3:c.3983+89T=	NP_000115.1:n.3983+89T=
XR_945953.1:n.243-10302A=
NM_001346440.1:c.3983+89T=	NP_001333369.1:n.3983+89T=
NM_000124.4:c.3983+89T= MANE Select	NP_000115.1:n.3983+89T=
NM_001346440.2:c.3983+89T=	NP_001333369.1:n.3983+89T=