Canonical Allele Identifier: CA2695198762

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138391513del , CM000667.2:g.138391513del	GRCh38
NC_000005.9:g.137727202del , CM000667.1:g.137727202del	GRCh37
NC_000005.8:g.137755101del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.1881del MANE Select	NP_057688.3:p.Lys627AsnfsTer?
ENST00000314358.10:c.1881del MANE Select	ENSP00000326563.5:p.Lys627AsnfsTer?
NM_016604.3:c.1881del	NP_057688.2:p.Lys627AsnfsTer?
ENST00000314358.9:c.1881del	ENSP00000326563.5:p.Lys627AsnfsTer?
ENST00000507996.5:c.46-1658del	ENSP00000423012.1:n.46-1658del
ENST00000510866.5:c.1591del	ENSP00000425186.1:n.1591del
ENST00000542866.2:c.-6-6834del	ENSP00000439462.2:n.-6-6834del
XM_005272018.3:c.1281del	XP_005272075.1:p.Lys427AsnfsTer?
XM_005272018.4:c.1281del	XP_005272075.1:p.Lys427AsnfsTer?
XM_011543488.1:c.1749del	XP_011541790.1:p.Lys583AsnfsTer?
XM_011543488.2:c.1749del	XP_011541790.1:p.Lys583AsnfsTer?
XM_011543489.1:c.1737del	XP_011541791.1:p.Lys579AsnfsTer?
XM_011543489.2:c.1737del	XP_011541791.1:p.Lys579AsnfsTer?
XM_017009584.1:c.1134del	XP_016865073.1:p.Lys378AsnfsTer?
XM_024446115.1:c.1407del	XP_024301883.1:p.Lys469AsnfsTer?