Canonical Allele Identifier: CA1240297894

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27479803_27479805delinsAAG , CM000664.2:g.27479803_27479805delinsAAG	GRCh38
NC_000002.11:g.27702670_27702672delinsAAG , CM000664.1:g.27702670_27702672delinsAAG	GRCh37
NC_000002.10:g.27556174_27556176delinsAAG	NCBI36
NG_034068.1:g.15007_15009delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.910-201_910-199delinsCTT MANE Select	ENSP00000260570.3:n.910-201_910-199delinsCTT
ENST00000476264.7:n.1199-201_1199-199delinsCTT
ENST00000674701.1:c.910-201_910-199delinsCTT	ENSP00000502275.1:n.910-201_910-199delinsCTT
ENST00000674824.1:c.847-201_847-199delinsCTT	ENSP00000501824.1:n.847-201_847-199delinsCTT
ENST00000674932.1:c.*573-201_*573-199delinsCTT	ENSP00000501967.1:n.*573-201_*573-199delinsCTT
ENST00000675410.1:c.229-201_229-199delinsCTT	ENSP00000502030.1:n.229-201_229-199delinsCTT
ENST00000675618.1:n.990-201_990-199delinsCTT
ENST00000675690.1:c.910-201_910-199delinsCTT	ENSP00000502283.1:n.910-201_910-199delinsCTT
ENST00000675728.1:c.847-201_847-199delinsCTT	ENSP00000501700.1:n.847-201_847-199delinsCTT
ENST00000675729.1:c.910-201_910-199delinsCTT	ENSP00000502319.1:n.910-201_910-199delinsCTT
ENST00000675963.1:c.*608-201_*608-199delinsCTT	ENSP00000502708.1:n.*608-201_*608-199delinsCTT
ENST00000676119.1:c.*200-201_*200-199delinsCTT	ENSP00000501701.1:n.*200-201_*200-199delinsCTT
ENST00000676300.1:n.996-201_996-199delinsCTT
ENST00000260570.7:c.910-201_910-199delinsCTT	ENSP00000260570.3:n.910-201_910-199delinsCTT
ENST00000359466.10:c.910-201_910-199delinsCTT	ENSP00000352443.6:n.910-201_910-199delinsCTT
ENST00000416524.2:c.847-201_847-199delinsCTT	ENSP00000407408.2:n.847-201_847-199delinsCTT
ENST00000476264.6:n.856-201_856-199delinsCTT
ENST00000507184.5:n.1042-201_1042-199delinsCTT
ENST00000511842.5:n.935-201_935-199delinsCTT
NM_015662.2:c.910-201_910-199delinsCTT	NP_056477.1:n.910-201_910-199delinsCTT
XM_005264254.1:c.910-201_910-199delinsCTT	XP_005264311.1:n.910-201_910-199delinsCTT
XM_006711986.2:c.847-201_847-199delinsCTT	XP_006712049.1:n.847-201_847-199delinsCTT
XM_006711987.1:c.910-201_910-199delinsCTT	XP_006712050.1:n.910-201_910-199delinsCTT
XM_011532757.1:c.229-201_229-199delinsCTT	XP_011531059.1:n.229-201_229-199delinsCTT
XM_011532758.1:c.910-201_910-199delinsCTT	XP_011531060.1:n.910-201_910-199delinsCTT
XM_006711986.3:c.847-201_847-199delinsCTT	XP_006712049.1:n.847-201_847-199delinsCTT
XM_011532757.2:c.229-201_229-199delinsCTT	XP_011531059.1:n.229-201_229-199delinsCTT
XM_017003790.1:c.847-201_847-199delinsCTT	XP_016859279.1:n.847-201_847-199delinsCTT
XM_017003791.1:c.229-201_229-199delinsCTT	XP_016859280.1:n.229-201_229-199delinsCTT
XM_017003792.1:c.910-201_910-199delinsCTT	XP_016859281.1:n.910-201_910-199delinsCTT
XM_017003793.1:c.-541-201_-541-199delinsCTT	XP_016859282.1:n.-541-201_-541-199delinsCTT
XM_017003794.1:c.-541-201_-541-199delinsCTT	XP_016859283.1:n.-541-201_-541-199delinsCTT
XM_017003795.1:c.-913-201_-913-199delinsCTT	XP_016859284.1:n.-913-201_-913-199delinsCTT
XR_001738698.1:n.965-201_965-199delinsCTT
NM_015662.3:c.910-201_910-199delinsCTT MANE Select	NP_056477.1:n.910-201_910-199delinsCTT