Canonical Allele Identifier: CA1139870447

Gene: ZNF678

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.227610249A= , CM000663.2:g.227610249A=	GRCh38
NC_000001.10:g.227797950A= , CM000663.1:g.227797950A=	GRCh37
NC_000001.9:g.225864573A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001367909.1:c.-163-36295A= MANE Select	NP_001354838.1:n.-163-36295A=
ENST00000343776.10:c.-163-36295A= MANE Select	ENSP00000344828.4:n.-163-36295A=
NM_001367910.1:c.-164+27643A=	NP_001354839.1:n.-164+27643A=
NM_001367911.1:c.31-36295A=	NP_001354840.1:n.31-36295A=
NM_178549.3:c.123+27643A=	NP_848644.2:n.123+27643A=
NM_178549.4:c.123+27643A=	NP_848644.2:n.123+27643A=
NR_033184.1:n.207-36295A=
NR_102302.1:n.299+27643A=
NR_102302.2:n.262+27643A=
ENST00000343776.9:c.-163-36295A=	ENSP00000344828.4:n.-163-36295A=
ENST00000440339.1:c.123+27643A=	ENSP00000394651.1:n.123+27643A=
ENST00000465266.1:n.267+27643A=
ENST00000608949.5:c.-164+27643A=	ENSP00000477097.1:n.-164+27643A=