Canonical Allele Identifier: CA1240297921

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27479873_27479874delinsCT , CM000664.2:g.27479873_27479874delinsCT	GRCh38
NC_000002.11:g.27702740_27702741delinsCT , CM000664.1:g.27702740_27702741delinsCT	GRCh37
NC_000002.10:g.27556244_27556245delinsCT	NCBI36
NG_034068.1:g.14938_14939delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.909+152_909+153delinsAG MANE Select	ENSP00000260570.3:n.909+152_909+153delinsAG
ENST00000476264.7:n.1198+152_1198+153delinsAG
ENST00000674701.1:c.909+152_909+153delinsAG	ENSP00000502275.1:n.909+152_909+153delinsAG
ENST00000674824.1:c.846+152_846+153delinsAG	ENSP00000501824.1:n.846+152_846+153delinsAG
ENST00000674932.1:c.*572+152_*572+153delinsAG	ENSP00000501967.1:n.*572+152_*572+153delinsAG
ENST00000675410.1:c.228+152_228+153delinsAG	ENSP00000502030.1:n.228+152_228+153delinsAG
ENST00000675618.1:n.989+152_989+153delinsAG
ENST00000675690.1:c.909+152_909+153delinsAG	ENSP00000502283.1:n.909+152_909+153delinsAG
ENST00000675728.1:c.846+152_846+153delinsAG	ENSP00000501700.1:n.846+152_846+153delinsAG
ENST00000675729.1:c.909+152_909+153delinsAG	ENSP00000502319.1:n.909+152_909+153delinsAG
ENST00000675963.1:c.*607+152_*607+153delinsAG	ENSP00000502708.1:n.*607+152_*607+153delinsAG
ENST00000676119.1:c.*199+152_*199+153delinsAG	ENSP00000501701.1:n.*199+152_*199+153delinsAG
ENST00000676300.1:n.995+152_995+153delinsAG
ENST00000260570.7:c.909+152_909+153delinsAG	ENSP00000260570.3:n.909+152_909+153delinsAG
ENST00000359466.10:c.909+152_909+153delinsAG	ENSP00000352443.6:n.909+152_909+153delinsAG
ENST00000416524.2:c.846+152_846+153delinsAG	ENSP00000407408.2:n.846+152_846+153delinsAG
ENST00000476264.6:n.855+152_855+153delinsAG
ENST00000507184.5:n.1041+152_1041+153delinsAG
ENST00000511842.5:n.934+152_934+153delinsAG
NM_015662.2:c.909+152_909+153delinsAG	NP_056477.1:n.909+152_909+153delinsAG
XM_005264254.1:c.909+152_909+153delinsAG	XP_005264311.1:n.909+152_909+153delinsAG
XM_006711986.2:c.846+152_846+153delinsAG	XP_006712049.1:n.846+152_846+153delinsAG
XM_006711987.1:c.909+152_909+153delinsAG	XP_006712050.1:n.909+152_909+153delinsAG
XM_011532757.1:c.228+152_228+153delinsAG	XP_011531059.1:n.228+152_228+153delinsAG
XM_011532758.1:c.909+152_909+153delinsAG	XP_011531060.1:n.909+152_909+153delinsAG
XM_006711986.3:c.846+152_846+153delinsAG	XP_006712049.1:n.846+152_846+153delinsAG
XM_011532757.2:c.228+152_228+153delinsAG	XP_011531059.1:n.228+152_228+153delinsAG
XM_017003790.1:c.846+152_846+153delinsAG	XP_016859279.1:n.846+152_846+153delinsAG
XM_017003791.1:c.228+152_228+153delinsAG	XP_016859280.1:n.228+152_228+153delinsAG
XM_017003792.1:c.909+152_909+153delinsAG	XP_016859281.1:n.909+152_909+153delinsAG
XM_017003793.1:c.-542+152_-542+153delinsAG	XP_016859282.1:n.-542+152_-542+153delinsAG
XM_017003794.1:c.-542+152_-542+153delinsAG	XP_016859283.1:n.-542+152_-542+153delinsAG
XM_017003795.1:c.-914+152_-914+153delinsAG	XP_016859284.1:n.-914+152_-914+153delinsAG
XR_001738698.1:n.964+152_964+153delinsAG
NM_015662.3:c.909+152_909+153delinsAG MANE Select	NP_056477.1:n.909+152_909+153delinsAG