Canonical Allele Identifier: CA352538841

Gene: KIF9 KIF9-AS1

Linked Data

• ClinVar Variation Id: 2331821
• ClinVar RCV Id: RCV004179063
• MyVariant Identifiers: chr3:g.47282305A>G (hg19) ; chr3:g.47240815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47240815A>G , CM000665.2:g.47240815A>G	GRCh38
NC_000003.11:g.47282305A>G , CM000665.1:g.47282305A>G	GRCh37
NC_000003.10:g.47257309A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684063.1:c.1910T>C (KIF9) MANE Select	ENSP00000507186.1:p.Leu637Pro
ENST00000265529.7:c.1910T>C (KIF9)	ENSP00000265529.3:p.Leu637Pro
ENST00000335044.6:c.1910T>C (KIF9)	ENSP00000333942.2:p.Leu637Pro
ENST00000444589.6:c.1715T>C (KIF9)	ENSP00000414987.2:p.Leu572Pro
ENST00000452770.6:c.1910T>C (KIF9)	ENSP00000391100.2:p.Leu637Pro
ENST00000487440.5:n.2268T>C (KIF9)
NM_001134878.1:c.1910T>C (KIF9)	NP_001128350.1:p.Leu637Pro
NM_022342.4:c.1715T>C (KIF9)	NP_071737.1:p.Leu572Pro
NM_182902.3:c.1910T>C (KIF9)	NP_878905.2:p.Leu637Pro
NR_033373.1:n.1402+621A>G (KIF9-AS1)
XM_005265388.3:c.2009T>C (KIF9)	XP_005265445.1:p.Leu670Pro
XM_005265389.3:c.1814T>C (KIF9)	XP_005265446.1:p.Leu605Pro
XM_006713291.2:c.1784T>C (KIF9)	XP_006713354.1:p.Leu595Pro
XM_011534003.1:c.1952T>C (KIF9)	XP_011532305.1:p.Leu651Pro
XM_011534004.1:c.1910T>C (KIF9)	XP_011532306.1:p.Leu637Pro
XM_011534005.1:c.1685T>C (KIF9)	XP_011532307.1:p.Leu562Pro
XM_011534006.1:c.1631T>C (KIF9)	XP_011532308.1:p.Leu544Pro
XM_011534007.1:c.941T>C (KIF9)	XP_011532309.1:p.Leu314Pro
XR_940488.1:n.2043T>C (KIF9)
XR_940489.1:n.1966T>C (KIF9)
XM_005265388.4:c.2009T>C (KIF9)	XP_005265445.1:p.Leu670Pro
XM_005265389.4:c.1814T>C (KIF9)	XP_005265446.1:p.Leu605Pro
XM_006713291.3:c.1784T>C (KIF9)	XP_006713354.1:p.Leu595Pro
XM_011534003.2:c.1952T>C (KIF9)	XP_011532305.1:p.Leu651Pro
XM_011534004.2:c.1910T>C (KIF9)	XP_011532306.1:p.Leu637Pro
XM_011534005.2:c.1685T>C (KIF9)	XP_011532307.1:p.Leu562Pro
XM_011534006.2:c.1631T>C (KIF9)	XP_011532308.1:p.Leu544Pro
XM_011534007.2:c.941T>C (KIF9)	XP_011532309.1:p.Leu314Pro
XM_017007029.1:c.1910T>C (KIF9)	XP_016862518.1:p.Leu637Pro
XM_017007030.1:c.1685T>C (KIF9)	XP_016862519.1:p.Leu562Pro
XM_017007031.1:c.1490T>C (KIF9)	XP_016862520.1:p.Leu497Pro
XR_002959567.1:n.1848T>C (KIF9)
XR_940488.2:n.2043T>C (KIF9)
XR_940489.2:n.1966T>C (KIF9)
NM_001134878.2:c.1910T>C (KIF9)	NP_001128350.1:p.Leu637Pro
NM_001377474.1:c.1685T>C (KIF9)	NP_001364403.1:p.Leu562Pro
NM_001377475.1:c.1490T>C (KIF9)	NP_001364404.1:p.Leu497Pro
NM_022342.5:c.1715T>C (KIF9)	NP_071737.1:p.Leu572Pro
NM_182902.4:c.1910T>C (KIF9) MANE Select	NP_878905.2:p.Leu637Pro
NM_001134878.3:c.1910T>C (KIF9)	NP_001128350.1:p.Leu637Pro
NM_022342.6:c.1715T>C (KIF9)	NP_071737.1:p.Leu572Pro