Canonical Allele Identifier: CA2749271334

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27480299_27480300insAG , CM000664.2:g.27480299_27480300insAG	GRCh38
NC_000002.11:g.27703166_27703167insAG , CM000664.1:g.27703166_27703167insAG	GRCh37
NC_000002.10:g.27556670_27556671insAG	NCBI36
NG_034068.1:g.14512_14513insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.786-151_786-150insCT MANE Select	ENSP00000260570.3:n.786-151_786-150insCT
ENST00000476264.7:n.1075-151_1075-150insCT
ENST00000674701.1:c.786-151_786-150insCT	ENSP00000502275.1:n.786-151_786-150insCT
ENST00000674824.1:c.723-151_723-150insCT	ENSP00000501824.1:n.723-151_723-150insCT
ENST00000674932.1:c.*449-151_*449-150insCT	ENSP00000501967.1:n.*449-151_*449-150insCT
ENST00000675410.1:c.105-151_105-150insCT	ENSP00000502030.1:n.105-151_105-150insCT
ENST00000675618.1:n.866-151_866-150insCT
ENST00000675690.1:c.786-151_786-150insCT	ENSP00000502283.1:n.786-151_786-150insCT
ENST00000675728.1:c.723-151_723-150insCT	ENSP00000501700.1:n.723-151_723-150insCT
ENST00000675729.1:c.786-151_786-150insCT	ENSP00000502319.1:n.786-151_786-150insCT
ENST00000675963.1:c.*484-151_*484-150insCT	ENSP00000502708.1:n.*484-151_*484-150insCT
ENST00000676119.1:c.*76-151_*76-150insCT	ENSP00000501701.1:n.*76-151_*76-150insCT
ENST00000676300.1:n.872-151_872-150insCT
ENST00000260570.7:c.786-151_786-150insCT	ENSP00000260570.3:n.786-151_786-150insCT
ENST00000359466.10:c.786-151_786-150insCT	ENSP00000352443.6:n.786-151_786-150insCT
ENST00000416524.2:c.723-151_723-150insCT	ENSP00000407408.2:n.723-151_723-150insCT
ENST00000476264.6:n.732-151_732-150insCT
ENST00000507184.5:n.918-151_918-150insCT
ENST00000511842.5:n.811-151_811-150insCT
NM_015662.2:c.786-151_786-150insCT	NP_056477.1:n.786-151_786-150insCT
XM_005264254.1:c.786-151_786-150insCT	XP_005264311.1:n.786-151_786-150insCT
XM_006711986.2:c.723-151_723-150insCT	XP_006712049.1:n.723-151_723-150insCT
XM_006711987.1:c.786-151_786-150insCT	XP_006712050.1:n.786-151_786-150insCT
XM_011532757.1:c.105-151_105-150insCT	XP_011531059.1:n.105-151_105-150insCT
XM_011532758.1:c.786-151_786-150insCT	XP_011531060.1:n.786-151_786-150insCT
XM_006711986.3:c.723-151_723-150insCT	XP_006712049.1:n.723-151_723-150insCT
XM_011532757.2:c.105-151_105-150insCT	XP_011531059.1:n.105-151_105-150insCT
XM_017003790.1:c.723-151_723-150insCT	XP_016859279.1:n.723-151_723-150insCT
XM_017003791.1:c.105-151_105-150insCT	XP_016859280.1:n.105-151_105-150insCT
XM_017003792.1:c.786-151_786-150insCT	XP_016859281.1:n.786-151_786-150insCT
XM_017003793.1:c.-665-151_-665-150insCT	XP_016859282.1:n.-665-151_-665-150insCT
XM_017003794.1:c.-665-151_-665-150insCT	XP_016859283.1:n.-665-151_-665-150insCT
XM_017003795.1:c.-1037-151_-1037-150insCT	XP_016859284.1:n.-1037-151_-1037-150insCT
XR_001738698.1:n.841-151_841-150insCT
NM_015662.3:c.786-151_786-150insCT MANE Select	NP_056477.1:n.786-151_786-150insCT