Canonical Allele Identifier: CA2749271323

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27480284_27480285insAT , CM000664.2:g.27480284_27480285insAT	GRCh38
NC_000002.11:g.27703151_27703152insAT , CM000664.1:g.27703151_27703152insAT	GRCh37
NC_000002.10:g.27556655_27556656insAT	NCBI36
NG_034068.1:g.14527_14528insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.786-136_786-135insAT MANE Select	ENSP00000260570.3:n.786-136_786-135insAT
ENST00000476264.7:n.1075-136_1075-135insAT
ENST00000674701.1:c.786-136_786-135insAT	ENSP00000502275.1:n.786-136_786-135insAT
ENST00000674824.1:c.723-136_723-135insAT	ENSP00000501824.1:n.723-136_723-135insAT
ENST00000674932.1:c.*449-136_*449-135insAT	ENSP00000501967.1:n.*449-136_*449-135insAT
ENST00000675410.1:c.105-136_105-135insAT	ENSP00000502030.1:n.105-136_105-135insAT
ENST00000675618.1:n.866-136_866-135insAT
ENST00000675690.1:c.786-136_786-135insAT	ENSP00000502283.1:n.786-136_786-135insAT
ENST00000675728.1:c.723-136_723-135insAT	ENSP00000501700.1:n.723-136_723-135insAT
ENST00000675729.1:c.786-136_786-135insAT	ENSP00000502319.1:n.786-136_786-135insAT
ENST00000675963.1:c.*484-136_*484-135insAT	ENSP00000502708.1:n.*484-136_*484-135insAT
ENST00000676119.1:c.*76-136_*76-135insAT	ENSP00000501701.1:n.*76-136_*76-135insAT
ENST00000676300.1:n.872-136_872-135insAT
ENST00000260570.7:c.786-136_786-135insAT	ENSP00000260570.3:n.786-136_786-135insAT
ENST00000359466.10:c.786-136_786-135insAT	ENSP00000352443.6:n.786-136_786-135insAT
ENST00000416524.2:c.723-136_723-135insAT	ENSP00000407408.2:n.723-136_723-135insAT
ENST00000476264.6:n.732-136_732-135insAT
ENST00000507184.5:n.918-136_918-135insAT
ENST00000511842.5:n.811-136_811-135insAT
NM_015662.2:c.786-136_786-135insAT	NP_056477.1:n.786-136_786-135insAT
XM_005264254.1:c.786-136_786-135insAT	XP_005264311.1:n.786-136_786-135insAT
XM_006711986.2:c.723-136_723-135insAT	XP_006712049.1:n.723-136_723-135insAT
XM_006711987.1:c.786-136_786-135insAT	XP_006712050.1:n.786-136_786-135insAT
XM_011532757.1:c.105-136_105-135insAT	XP_011531059.1:n.105-136_105-135insAT
XM_011532758.1:c.786-136_786-135insAT	XP_011531060.1:n.786-136_786-135insAT
XM_006711986.3:c.723-136_723-135insAT	XP_006712049.1:n.723-136_723-135insAT
XM_011532757.2:c.105-136_105-135insAT	XP_011531059.1:n.105-136_105-135insAT
XM_017003790.1:c.723-136_723-135insAT	XP_016859279.1:n.723-136_723-135insAT
XM_017003791.1:c.105-136_105-135insAT	XP_016859280.1:n.105-136_105-135insAT
XM_017003792.1:c.786-136_786-135insAT	XP_016859281.1:n.786-136_786-135insAT
XM_017003793.1:c.-665-136_-665-135insAT	XP_016859282.1:n.-665-136_-665-135insAT
XM_017003794.1:c.-665-136_-665-135insAT	XP_016859283.1:n.-665-136_-665-135insAT
XM_017003795.1:c.-1037-136_-1037-135insAT	XP_016859284.1:n.-1037-136_-1037-135insAT
XR_001738698.1:n.841-136_841-135insAT
NM_015662.3:c.786-136_786-135insAT MANE Select	NP_056477.1:n.786-136_786-135insAT