Canonical Allele Identifier: CA2838403937

Gene: ZNF678

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.227616363C>A , CM000663.2:g.227616363C>A	GRCh38
NC_000001.10:g.227804064C>A , CM000663.1:g.227804064C>A	GRCh37
NC_000001.9:g.225870687C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343776.10:c.-163-30181C>A MANE Select	ENSP00000344828.4:n.-163-30181C>A
ENST00000343776.9:c.-163-30181C>A	ENSP00000344828.4:n.-163-30181C>A
ENST00000440339.1:c.124-30181C>A	ENSP00000394651.1:n.124-30181C>A
ENST00000465266.1:n.268-30181C>A
ENST00000608949.5:c.-163-30181C>A	ENSP00000477097.1:n.-163-30181C>A
NM_178549.3:c.124-30181C>A	NP_848644.2:n.124-30181C>A
NR_033184.1:n.207-30181C>A
NR_102302.1:n.300-30181C>A
NM_001367909.1:c.-163-30181C>A MANE Select	NP_001354838.1:n.-163-30181C>A
NM_001367910.1:c.-163-30181C>A	NP_001354839.1:n.-163-30181C>A
NM_001367911.1:c.31-30181C>A	NP_001354840.1:n.31-30181C>A
NM_178549.4:c.124-30181C>A	NP_848644.2:n.124-30181C>A
NR_102302.2:n.263-30181C>A