Canonical Allele Identifier: CA1240296888
Gene: IFT172 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27477315G= , CM000664.2:g.27477315G= GRCh38
NC_000002.11:g.27700182G= , CM000664.1:g.27700182G= GRCh37
NC_000002.10:g.27553686G= NCBI36
NG_034068.1:g.17497C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260570.8:c.1227C= MANE Select ENSP00000260570.3:p.Cys409=
ENST00000476264.7:n.1516C=
ENST00000674701.1:c.1227C= ENSP00000502275.1:p.Cys409=
ENST00000674824.1:c.1164C= ENSP00000501824.1:p.Cys388=
ENST00000674932.1:c.*890C= ENSP00000501967.1:n.*890C=
ENST00000675410.1:c.546C= ENSP00000502030.1:p.Cys182=
ENST00000675618.1:n.1307C=
ENST00000675690.1:c.1227C= ENSP00000502283.1:p.Cys409=
ENST00000675728.1:c.1164C= ENSP00000501700.1:p.Cys388=
ENST00000675729.1:c.1227C= ENSP00000502319.1:p.Cys409=
ENST00000675963.1:c.*925C= ENSP00000502708.1:n.*925C=
ENST00000676119.1:c.*517C= ENSP00000501701.1:n.*517C=
ENST00000676300.1:n.1551C=
ENST00000260570.7:c.1227C= ENSP00000260570.3:p.Cys409=
ENST00000359466.10:c.1227C= ENSP00000352443.6:p.Cys409=
ENST00000416524.2:c.1164C= ENSP00000407408.2:p.Cys388=
ENST00000476264.6:n.1173C=
ENST00000507184.5:n.1359C=
ENST00000511842.5:n.1252C=
NM_015662.2:c.1227C= NP_056477.1:p.Cys409=
XM_005264254.1:c.1227C= XP_005264311.1:p.Cys409=
XM_006711986.2:c.1164C= XP_006712049.1:p.Cys388=
XM_006711987.1:c.1227C= XP_006712050.1:p.Cys409=
XM_011532757.1:c.546C= XP_011531059.1:p.Cys182=
XM_011532758.1:c.1227C= XP_011531060.1:p.Cys409=
XM_006711986.3:c.1164C= XP_006712049.1:p.Cys388=
XM_011532757.2:c.546C= XP_011531059.1:p.Cys182=
XM_017003790.1:c.1164C= XP_016859279.1:p.Cys388=
XM_017003791.1:c.546C= XP_016859280.1:p.Cys182=
XM_017003792.1:c.1227C= XP_016859281.1:p.Cys409=
XM_017003793.1:c.-224C= XP_016859282.1:n.-224C=
XM_017003794.1:c.-224C= XP_016859283.1:n.-224C=
XM_017003795.1:c.-596C= XP_016859284.1:n.-596C=
XR_001738698.1:n.1282C=
NM_015662.3:c.1227C= MANE Select NP_056477.1:p.Cys409=