Canonical Allele Identifier: CA2577139998

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27480208_27480209del , CM000664.2:g.27480208_27480209del	GRCh38
NC_000002.11:g.27703075_27703076del , CM000664.1:g.27703075_27703076del	GRCh37
NC_000002.10:g.27556579_27556580del	NCBI36
NG_034068.1:g.14604_14605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.786-59_786-58del MANE Select	ENSP00000260570.3:n.786-59_786-58del
ENST00000476264.7:n.1075-59_1075-58del
ENST00000674701.1:c.786-59_786-58del	ENSP00000502275.1:n.786-59_786-58del
ENST00000674824.1:c.723-59_723-58del	ENSP00000501824.1:n.723-59_723-58del
ENST00000674932.1:c.*449-59_*449-58del	ENSP00000501967.1:n.*449-59_*449-58del
ENST00000675410.1:c.105-59_105-58del	ENSP00000502030.1:n.105-59_105-58del
ENST00000675618.1:n.866-59_866-58del
ENST00000675690.1:c.786-59_786-58del	ENSP00000502283.1:n.786-59_786-58del
ENST00000675728.1:c.723-59_723-58del	ENSP00000501700.1:n.723-59_723-58del
ENST00000675729.1:c.786-59_786-58del	ENSP00000502319.1:n.786-59_786-58del
ENST00000675963.1:c.*484-59_*484-58del	ENSP00000502708.1:n.*484-59_*484-58del
ENST00000676119.1:c.*76-59_*76-58del	ENSP00000501701.1:n.*76-59_*76-58del
ENST00000676300.1:n.872-59_872-58del
ENST00000260570.7:c.786-59_786-58del	ENSP00000260570.3:n.786-59_786-58del
ENST00000359466.10:c.786-59_786-58del	ENSP00000352443.6:n.786-59_786-58del
ENST00000416524.2:c.723-59_723-58del	ENSP00000407408.2:n.723-59_723-58del
ENST00000476264.6:n.732-59_732-58del
ENST00000507184.5:n.918-59_918-58del
ENST00000511842.5:n.811-59_811-58del
NM_015662.2:c.786-59_786-58del	NP_056477.1:n.786-59_786-58del
XM_005264254.1:c.786-59_786-58del	XP_005264311.1:n.786-59_786-58del
XM_006711986.2:c.723-59_723-58del	XP_006712049.1:n.723-59_723-58del
XM_006711987.1:c.786-59_786-58del	XP_006712050.1:n.786-59_786-58del
XM_011532757.1:c.105-59_105-58del	XP_011531059.1:n.105-59_105-58del
XM_011532758.1:c.786-59_786-58del	XP_011531060.1:n.786-59_786-58del
XM_006711986.3:c.723-59_723-58del	XP_006712049.1:n.723-59_723-58del
XM_011532757.2:c.105-59_105-58del	XP_011531059.1:n.105-59_105-58del
XM_017003790.1:c.723-59_723-58del	XP_016859279.1:n.723-59_723-58del
XM_017003791.1:c.105-59_105-58del	XP_016859280.1:n.105-59_105-58del
XM_017003792.1:c.786-59_786-58del	XP_016859281.1:n.786-59_786-58del
XM_017003793.1:c.-665-59_-665-58del	XP_016859282.1:n.-665-59_-665-58del
XM_017003794.1:c.-665-59_-665-58del	XP_016859283.1:n.-665-59_-665-58del
XM_017003795.1:c.-1037-59_-1037-58del	XP_016859284.1:n.-1037-59_-1037-58del
XR_001738698.1:n.841-59_841-58del
NM_015662.3:c.786-59_786-58del MANE Select	NP_056477.1:n.786-59_786-58del