Canonical Allele Identifier: CA346396834
Gene: IFT172 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27480036C>A , CM000664.2:g.27480036C>A GRCh38
NC_000002.11:g.27702903C>A , CM000664.1:g.27702903C>A GRCh37
NC_000002.10:g.27556407C>A NCBI36
NG_034068.1:g.14776G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260570.8:c.899G>T MANE Select ENSP00000260570.3:p.Arg300Leu
ENST00000476264.7:n.1188G>T
ENST00000674701.1:c.899G>T ENSP00000502275.1:p.Arg300Leu
ENST00000674824.1:c.836G>T ENSP00000501824.1:p.Arg279Leu
ENST00000674932.1:c.*562G>T ENSP00000501967.1:n.*562G>T
ENST00000675410.1:c.218G>T ENSP00000502030.1:p.Arg73Leu
ENST00000675618.1:n.979G>T
ENST00000675690.1:c.899G>T ENSP00000502283.1:p.Arg300Leu
ENST00000675728.1:c.836G>T ENSP00000501700.1:p.Arg279Leu
ENST00000675729.1:c.899G>T ENSP00000502319.1:p.Arg300Leu
ENST00000675963.1:c.*597G>T ENSP00000502708.1:n.*597G>T
ENST00000676119.1:c.*189G>T ENSP00000501701.1:n.*189G>T
ENST00000676300.1:n.985G>T
ENST00000260570.7:c.899G>T ENSP00000260570.3:p.Arg300Leu
ENST00000359466.10:c.899G>T ENSP00000352443.6:p.Arg300Leu
ENST00000416524.2:c.836G>T ENSP00000407408.2:p.Arg279Leu
ENST00000476264.6:n.845G>T
ENST00000507184.5:n.1031G>T
ENST00000511842.5:n.924G>T
NM_015662.2:c.899G>T NP_056477.1:p.Arg300Leu
XM_005264254.1:c.899G>T XP_005264311.1:p.Arg300Leu
XM_006711986.2:c.836G>T XP_006712049.1:p.Arg279Leu
XM_006711987.1:c.899G>T XP_006712050.1:p.Arg300Leu
XM_011532757.1:c.218G>T XP_011531059.1:p.Arg73Leu
XM_011532758.1:c.899G>T XP_011531060.1:p.Arg300Leu
XM_006711986.3:c.836G>T XP_006712049.1:p.Arg279Leu
XM_011532757.2:c.218G>T XP_011531059.1:p.Arg73Leu
XM_017003790.1:c.836G>T XP_016859279.1:p.Arg279Leu
XM_017003791.1:c.218G>T XP_016859280.1:p.Arg73Leu
XM_017003792.1:c.899G>T XP_016859281.1:p.Arg300Leu
XM_017003793.1:c.-552G>T XP_016859282.1:n.-552G>T
XM_017003794.1:c.-552G>T XP_016859283.1:n.-552G>T
XM_017003795.1:c.-924G>T XP_016859284.1:n.-924G>T
XR_001738698.1:n.954G>T
NM_015662.3:c.899G>T MANE Select NP_056477.1:p.Arg300Leu