Canonical Allele Identifier: CA11550948
Gene: KIF9 HGNC NCBI

Linked Data

dbSNP Id: rs1076394
gnomAD v2: 3-47322781-G-A
gnomAD v3: 3-47281291-G-A
gnomAD v4: 3-47281291-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47281291G>A , CM000665.2:g.47281291G>A GRCh38
NC_000003.11:g.47322781G>A , CM000665.1:g.47322781G>A GRCh37
NC_000003.10:g.47297785G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000684063.1:c.-6+1204C>T MANE Select ENSP00000507186.1:n.-6+1204C>T
ENST00000265529.7:c.-6+1204C>T ENSP00000265529.3:n.-6+1204C>T
ENST00000335044.6:c.-6+1204C>T ENSP00000333942.2:n.-6+1204C>T
ENST00000425452.1:c.-207-96C>T ENSP00000406603.1:n.-207-96C>T
ENST00000425853.5:c.-6+849C>T ENSP00000406815.1:n.-6+849C>T
ENST00000432493.5:c.-6+1204C>T ENSP00000391099.1:n.-6+1204C>T
ENST00000443784.5:c.-6+1204C>T ENSP00000405774.1:n.-6+1204C>T
ENST00000444589.6:c.-6+1204C>T ENSP00000414987.2:n.-6+1204C>T
ENST00000452770.6:c.-6+849C>T ENSP00000391100.2:n.-6+849C>T
ENST00000456548.5:c.-6+1204C>T ENSP00000387959.1:n.-6+1204C>T
ENST00000487440.5:n.353+1204C>T
ENST00000498584.1:n.272+1204C>T
NM_001134878.1:c.-6+849C>T NP_001128350.1:n.-6+849C>T
NM_022342.4:c.-6+1204C>T NP_071737.1:n.-6+1204C>T
NM_182902.3:c.-6+1204C>T NP_878905.2:n.-6+1204C>T
XM_005265388.3:c.98+1204C>T XP_005265445.1:n.98+1204C>T
XM_005265389.3:c.98+1204C>T XP_005265446.1:n.98+1204C>T
XM_006713291.2:c.98+1204C>T XP_006713354.1:n.98+1204C>T
XM_011534003.1:c.-303C>T XP_011532305.1:n.-303C>T
XM_011534004.1:c.-2+849C>T XP_011532306.1:n.-2+849C>T
XM_011534005.1:c.-6+1204C>T XP_011532307.1:n.-6+1204C>T
XM_011534006.1:c.-178+1204C>T XP_011532308.1:n.-178+1204C>T
XR_940488.1:n.132+1204C>T
XR_940489.1:n.353+1204C>T
XM_005265388.4:c.98+1204C>T XP_005265445.1:n.98+1204C>T
XM_005265389.4:c.98+1204C>T XP_005265446.1:n.98+1204C>T
XM_006713291.3:c.98+1204C>T XP_006713354.1:n.98+1204C>T
XM_011534003.2:c.-207-96C>T XP_011532305.1:n.-207-96C>T
XM_011534004.2:c.-2+849C>T XP_011532306.1:n.-2+849C>T
XM_011534005.2:c.-6+1204C>T XP_011532307.1:n.-6+1204C>T
XM_011534006.2:c.-178+1204C>T XP_011532308.1:n.-178+1204C>T
XM_017007029.1:c.-245-96C>T XP_016862518.1:n.-245-96C>T
XM_017007030.1:c.-2+849C>T XP_016862519.1:n.-2+849C>T
XM_017007031.1:c.-6+1204C>T XP_016862520.1:n.-6+1204C>T
XR_002959567.1:n.132+1204C>T
XR_940488.2:n.132+1204C>T
XR_940489.2:n.353+1204C>T
NM_001134878.2:c.-6+849C>T NP_001128350.1:n.-6+849C>T
NM_001377474.1:c.-6+1204C>T NP_001364403.1:n.-6+1204C>T
NM_001377475.1:c.-6+1204C>T NP_001364404.1:n.-6+1204C>T
NM_001377476.1:c.-6+1204C>T NP_001364405.1:n.-6+1204C>T
NM_001377477.1:c.-6+849C>T NP_001364406.1:n.-6+849C>T
NM_022342.5:c.-6+1204C>T NP_071737.1:n.-6+1204C>T
NM_182902.4:c.-6+1204C>T MANE Select NP_878905.2:n.-6+1204C>T
NM_001134878.3:c.-6+849C>T NP_001128350.1:n.-6+849C>T
NM_022342.6:c.-6+1204C>T NP_071737.1:n.-6+1204C>T