Canonical Allele Identifier: CA2749271273

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27479780_27479782del , CM000664.2:g.27479780_27479782del	GRCh38
NC_000002.11:g.27702647_27702649del , CM000664.1:g.27702647_27702649del	GRCh37
NC_000002.10:g.27556151_27556153del	NCBI36
NG_034068.1:g.15030_15032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.910-178_910-176del MANE Select	ENSP00000260570.3:n.910-178_910-176del
ENST00000476264.7:n.1199-178_1199-176del
ENST00000674701.1:c.910-178_910-176del	ENSP00000502275.1:n.910-178_910-176del
ENST00000674824.1:c.847-178_847-176del	ENSP00000501824.1:n.847-178_847-176del
ENST00000674932.1:c.*573-178_*573-176del	ENSP00000501967.1:n.*573-178_*573-176del
ENST00000675410.1:c.229-178_229-176del	ENSP00000502030.1:n.229-178_229-176del
ENST00000675618.1:n.990-178_990-176del
ENST00000675690.1:c.910-178_910-176del	ENSP00000502283.1:n.910-178_910-176del
ENST00000675728.1:c.847-178_847-176del	ENSP00000501700.1:n.847-178_847-176del
ENST00000675729.1:c.910-178_910-176del	ENSP00000502319.1:n.910-178_910-176del
ENST00000675963.1:c.*608-178_*608-176del	ENSP00000502708.1:n.*608-178_*608-176del
ENST00000676119.1:c.*200-178_*200-176del	ENSP00000501701.1:n.*200-178_*200-176del
ENST00000676300.1:n.996-178_996-176del
ENST00000260570.7:c.910-178_910-176del	ENSP00000260570.3:n.910-178_910-176del
ENST00000359466.10:c.910-178_910-176del	ENSP00000352443.6:n.910-178_910-176del
ENST00000416524.2:c.847-178_847-176del	ENSP00000407408.2:n.847-178_847-176del
ENST00000476264.6:n.856-178_856-176del
ENST00000507184.5:n.1042-178_1042-176del
ENST00000511842.5:n.935-178_935-176del
NM_015662.2:c.910-178_910-176del	NP_056477.1:n.910-178_910-176del
XM_005264254.1:c.910-178_910-176del	XP_005264311.1:n.910-178_910-176del
XM_006711986.2:c.847-178_847-176del	XP_006712049.1:n.847-178_847-176del
XM_006711987.1:c.910-178_910-176del	XP_006712050.1:n.910-178_910-176del
XM_011532757.1:c.229-178_229-176del	XP_011531059.1:n.229-178_229-176del
XM_011532758.1:c.910-178_910-176del	XP_011531060.1:n.910-178_910-176del
XM_006711986.3:c.847-178_847-176del	XP_006712049.1:n.847-178_847-176del
XM_011532757.2:c.229-178_229-176del	XP_011531059.1:n.229-178_229-176del
XM_017003790.1:c.847-178_847-176del	XP_016859279.1:n.847-178_847-176del
XM_017003791.1:c.229-178_229-176del	XP_016859280.1:n.229-178_229-176del
XM_017003792.1:c.910-178_910-176del	XP_016859281.1:n.910-178_910-176del
XM_017003793.1:c.-541-178_-541-176del	XP_016859282.1:n.-541-178_-541-176del
XM_017003794.1:c.-541-178_-541-176del	XP_016859283.1:n.-541-178_-541-176del
XM_017003795.1:c.-913-178_-913-176del	XP_016859284.1:n.-913-178_-913-176del
XR_001738698.1:n.965-178_965-176del
NM_015662.3:c.910-178_910-176del MANE Select	NP_056477.1:n.910-178_910-176del