Canonical Allele Identifier: CA1240297904
Gene: IFT172 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27479837T= , CM000664.2:g.27479837T= GRCh38
NC_000002.11:g.27702704T= , CM000664.1:g.27702704T= GRCh37
NC_000002.10:g.27556208T= NCBI36
NG_034068.1:g.14975A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260570.8:c.909+189A= MANE Select ENSP00000260570.3:n.909+189A=
ENST00000476264.7:n.1198+189A=
ENST00000674701.1:c.909+189A= ENSP00000502275.1:n.909+189A=
ENST00000674824.1:c.846+189A= ENSP00000501824.1:n.846+189A=
ENST00000674932.1:c.*572+189A= ENSP00000501967.1:n.*572+189A=
ENST00000675410.1:c.228+189A= ENSP00000502030.1:n.228+189A=
ENST00000675618.1:n.989+189A=
ENST00000675690.1:c.909+189A= ENSP00000502283.1:n.909+189A=
ENST00000675728.1:c.846+189A= ENSP00000501700.1:n.846+189A=
ENST00000675729.1:c.909+189A= ENSP00000502319.1:n.909+189A=
ENST00000675963.1:c.*607+189A= ENSP00000502708.1:n.*607+189A=
ENST00000676119.1:c.*199+189A= ENSP00000501701.1:n.*199+189A=
ENST00000676300.1:n.995+189A=
ENST00000260570.7:c.909+189A= ENSP00000260570.3:n.909+189A=
ENST00000359466.10:c.909+189A= ENSP00000352443.6:n.909+189A=
ENST00000416524.2:c.846+189A= ENSP00000407408.2:n.846+189A=
ENST00000476264.6:n.855+189A=
ENST00000507184.5:n.1041+189A=
ENST00000511842.5:n.934+189A=
NM_015662.2:c.909+189A= NP_056477.1:n.909+189A=
XM_005264254.1:c.909+189A= XP_005264311.1:n.909+189A=
XM_006711986.2:c.846+189A= XP_006712049.1:n.846+189A=
XM_006711987.1:c.909+189A= XP_006712050.1:n.909+189A=
XM_011532757.1:c.228+189A= XP_011531059.1:n.228+189A=
XM_011532758.1:c.909+189A= XP_011531060.1:n.909+189A=
XM_006711986.3:c.846+189A= XP_006712049.1:n.846+189A=
XM_011532757.2:c.228+189A= XP_011531059.1:n.228+189A=
XM_017003790.1:c.846+189A= XP_016859279.1:n.846+189A=
XM_017003791.1:c.228+189A= XP_016859280.1:n.228+189A=
XM_017003792.1:c.909+189A= XP_016859281.1:n.909+189A=
XM_017003793.1:c.-542+189A= XP_016859282.1:n.-542+189A=
XM_017003794.1:c.-542+189A= XP_016859283.1:n.-542+189A=
XM_017003795.1:c.-914+189A= XP_016859284.1:n.-914+189A=
XR_001738698.1:n.964+189A=
NM_015662.3:c.909+189A= MANE Select NP_056477.1:n.909+189A=