Canonical Allele Identifier: CA1240297937

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27479912_27479913delinsCA , CM000664.2:g.27479912_27479913delinsCA	GRCh38
NC_000002.11:g.27702779_27702780delinsCA , CM000664.1:g.27702779_27702780delinsCA	GRCh37
NC_000002.10:g.27556283_27556284delinsCA	NCBI36
NG_034068.1:g.14899_14900delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.909+113_909+114delinsTG MANE Select	ENSP00000260570.3:n.909+113_909+114delinsTG
ENST00000476264.7:n.1198+113_1198+114delinsTG
ENST00000674701.1:c.909+113_909+114delinsTG	ENSP00000502275.1:n.909+113_909+114delinsTG
ENST00000674824.1:c.846+113_846+114delinsTG	ENSP00000501824.1:n.846+113_846+114delinsTG
ENST00000674932.1:c.*572+113_*572+114delinsTG	ENSP00000501967.1:n.*572+113_*572+114delinsTG
ENST00000675410.1:c.228+113_228+114delinsTG	ENSP00000502030.1:n.228+113_228+114delinsTG
ENST00000675618.1:n.989+113_989+114delinsTG
ENST00000675690.1:c.909+113_909+114delinsTG	ENSP00000502283.1:n.909+113_909+114delinsTG
ENST00000675728.1:c.846+113_846+114delinsTG	ENSP00000501700.1:n.846+113_846+114delinsTG
ENST00000675729.1:c.909+113_909+114delinsTG	ENSP00000502319.1:n.909+113_909+114delinsTG
ENST00000675963.1:c.*607+113_*607+114delinsTG	ENSP00000502708.1:n.*607+113_*607+114delinsTG
ENST00000676119.1:c.*199+113_*199+114delinsTG	ENSP00000501701.1:n.*199+113_*199+114delinsTG
ENST00000676300.1:n.995+113_995+114delinsTG
ENST00000260570.7:c.909+113_909+114delinsTG	ENSP00000260570.3:n.909+113_909+114delinsTG
ENST00000359466.10:c.909+113_909+114delinsTG	ENSP00000352443.6:n.909+113_909+114delinsTG
ENST00000416524.2:c.846+113_846+114delinsTG	ENSP00000407408.2:n.846+113_846+114delinsTG
ENST00000476264.6:n.855+113_855+114delinsTG
ENST00000507184.5:n.1041+113_1041+114delinsTG
ENST00000511842.5:n.934+113_934+114delinsTG
NM_015662.2:c.909+113_909+114delinsTG	NP_056477.1:n.909+113_909+114delinsTG
XM_005264254.1:c.909+113_909+114delinsTG	XP_005264311.1:n.909+113_909+114delinsTG
XM_006711986.2:c.846+113_846+114delinsTG	XP_006712049.1:n.846+113_846+114delinsTG
XM_006711987.1:c.909+113_909+114delinsTG	XP_006712050.1:n.909+113_909+114delinsTG
XM_011532757.1:c.228+113_228+114delinsTG	XP_011531059.1:n.228+113_228+114delinsTG
XM_011532758.1:c.909+113_909+114delinsTG	XP_011531060.1:n.909+113_909+114delinsTG
XM_006711986.3:c.846+113_846+114delinsTG	XP_006712049.1:n.846+113_846+114delinsTG
XM_011532757.2:c.228+113_228+114delinsTG	XP_011531059.1:n.228+113_228+114delinsTG
XM_017003790.1:c.846+113_846+114delinsTG	XP_016859279.1:n.846+113_846+114delinsTG
XM_017003791.1:c.228+113_228+114delinsTG	XP_016859280.1:n.228+113_228+114delinsTG
XM_017003792.1:c.909+113_909+114delinsTG	XP_016859281.1:n.909+113_909+114delinsTG
XM_017003793.1:c.-542+113_-542+114delinsTG	XP_016859282.1:n.-542+113_-542+114delinsTG
XM_017003794.1:c.-542+113_-542+114delinsTG	XP_016859283.1:n.-542+113_-542+114delinsTG
XM_017003795.1:c.-914+113_-914+114delinsTG	XP_016859284.1:n.-914+113_-914+114delinsTG
XR_001738698.1:n.964+113_964+114delinsTG
NM_015662.3:c.909+113_909+114delinsTG MANE Select	NP_056477.1:n.909+113_909+114delinsTG