Canonical Allele Identifier: CA634372023
Gene: KIF16B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.16555769C>G , CM000682.2:g.16555769C>G GRCh38
NC_000020.10:g.16536414C>G , CM000682.1:g.16536414C>G GRCh37
NC_000020.9:g.16484414C>G NCBI36
NG_028043.1:g.22666G>C
NG_028043.2:g.22666G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000635823.2:c.47+17460G>C ENSP00000490639.2:n.47+17460G>C
ENST00000354981.7:c.47+17460G>C MANE Select ENSP00000347076.2:n.47+17460G>C
ENST00000636835.1:c.47+17460G>C ENSP00000489838.1:n.47+17460G>C
ENST00000354981.6:c.47+17460G>C ENSP00000347076.2:n.47+17460G>C
ENST00000408042.5:c.47+17460G>C ENSP00000384164.1:n.47+17460G>C
NM_001199865.1:c.47+17460G>C NP_001186794.1:n.47+17460G>C
NM_001199866.1:c.47+17460G>C NP_001186795.1:n.47+17460G>C
NM_024704.4:c.47+17460G>C NP_078980.3:n.47+17460G>C
XM_005260750.2:c.47+17460G>C XP_005260807.1:n.47+17460G>C
XM_005260751.3:c.47+17460G>C XP_005260808.1:n.47+17460G>C
XM_005260752.2:c.47+17460G>C XP_005260809.1:n.47+17460G>C
XM_005260753.2:c.47+17460G>C XP_005260810.1:n.47+17460G>C
XM_005260754.2:c.47+17460G>C XP_005260811.1:n.47+17460G>C
XM_005260755.2:c.47+17460G>C XP_005260812.1:n.47+17460G>C
XM_006723588.2:c.47+17460G>C XP_006723651.1:n.47+17460G>C
XM_011529288.1:c.47+17460G>C XP_011527590.1:n.47+17460G>C
XM_005260750.3:c.47+17460G>C XP_005260807.1:n.47+17460G>C
XM_005260751.4:c.47+17460G>C XP_005260808.1:n.47+17460G>C
XM_005260752.3:c.47+17460G>C XP_005260809.1:n.47+17460G>C
XM_005260753.3:c.47+17460G>C XP_005260810.1:n.47+17460G>C
XM_005260754.3:c.47+17460G>C XP_005260811.1:n.47+17460G>C
XM_005260755.3:c.47+17460G>C XP_005260812.1:n.47+17460G>C
XM_006723588.3:c.47+17460G>C XP_006723651.1:n.47+17460G>C
XM_017027926.1:c.47+17460G>C XP_016883415.1:n.47+17460G>C
NM_001199865.2:c.47+17460G>C NP_001186794.1:n.47+17460G>C
NM_001199866.2:c.47+17460G>C NP_001186795.1:n.47+17460G>C
NM_024704.5:c.47+17460G>C MANE Select NP_078980.3:n.47+17460G>C
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