Canonical Allele Identifier: CA5032135

Gene: KIF24

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34259656T>C , CM000671.2:g.34259656T>C	GRCh38
NC_000009.11:g.34259654T>C , CM000671.1:g.34259654T>C	GRCh37
NC_000009.10:g.34249654T>C	NCBI36
NG_053094.1:g.78317A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_194313.4:c.1565A>G MANE Select	NP_919289.2:p.Asn522Ser
ENST00000402558.7:c.1565A>G MANE Select	ENSP00000384433.1:p.Asn522Ser
NM_194313.2:c.1565A>G	NP_919289.2:p.Asn522Ser
NM_194313.3:c.1565A>G	NP_919289.2:p.Asn522Ser
ENST00000379166.2:c.1565A>G	ENSP00000368464.2:p.Asn522Ser
ENST00000379174.7:c.1163A>G	ENSP00000368472.3:p.Asn388Ser
ENST00000402558.6:c.1565A>G	ENSP00000384433.1:p.Asn522Ser
XM_005251450.2:c.698A>G	XP_005251507.1:p.Asn233Ser
XM_005251451.2:c.482A>G	XP_005251508.1:p.Asn161Ser
XM_006716764.2:c.191A>G	XP_006716827.1:p.Asn64Ser
XM_006716764.3:c.191A>G	XP_006716827.1:p.Asn64Ser
XM_011517860.1:c.1658A>G	XP_011516162.1:p.Asn553Ser
XM_011517861.1:c.1658A>G	XP_011516163.1:p.Asn553Ser
XM_011517861.2:c.1658A>G	XP_011516163.1:p.Asn553Ser
XM_011517862.1:c.1658A>G	XP_011516164.1:p.Asn553Ser
XM_011517863.1:c.1565A>G	XP_011516165.1:p.Asn522Ser
XM_011517863.3:c.1565A>G	XP_011516165.1:p.Asn522Ser
XM_017014697.2:c.1565A>G	XP_016870186.1:p.Asn522Ser
XM_017014698.2:c.698A>G	XP_016870187.1:p.Asn233Ser
XM_024447533.1:c.482A>G	XP_024303301.1:p.Asn161Ser