Canonical Allele Identifier: CA2334456311

Gene: ZNF585B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.37194064A>C , CM000681.2:g.37194064A>C	GRCh38
NC_000019.9:g.37684966A>C , CM000681.1:g.37684966A>C	GRCh37
NC_000019.8:g.42376806A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532828.7:c.73-3914T>G MANE Select	ENSP00000433773.1:n.73-3914T>G
ENST00000586320.2:c.71-3914T>G
ENST00000392156.7:c.*18-3914T>G	ENSP00000432760.1:n.*18-3914T>G
ENST00000526705.1:c.*179-3914T>G	ENSP00000434541.1:n.*179-3914T>G
ENST00000527838.5:c.73-3914T>G	ENSP00000435268.1:n.73-3914T>G
ENST00000532828.6:c.73-3914T>G	ENSP00000433773.1:n.73-3914T>G
ENST00000585860.2:c.73-3914T>G	ENSP00000465960.1:n.73-3914T>G
ENST00000586320.1:c.28-3914T>G	ENSP00000467380.1:n.28-3914T>G
ENST00000588873.1:c.35+12976T>G
ENST00000590245.5:c.*164+1817T>G	ENSP00000467945.1:n.*164+1817T>G
ENST00000591273.5:c.*28+1817T>G	ENSP00000467283.1:n.*28+1817T>G
ENST00000591492.5:c.28-3914T>G	ENSP00000465871.1:n.28-3914T>G
NM_152279.3:c.73-3914T>G	NP_689492.3:n.73-3914T>G
NM_152279.4:c.73-3914T>G MANE Select	NP_689492.3:n.73-3914T>G