Canonical Allele Identifier: CA346380931

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27457978T>A , CM000664.2:g.27457978T>A	GRCh38
NC_000002.11:g.27680845T>A , CM000664.1:g.27680845T>A	GRCh37
NC_000002.10:g.27534349T>A	NCBI36
NG_034068.1:g.36834A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015662.3:c.2976-2A>T MANE Select	NP_056477.1:n.2976-2A>T
ENST00000260570.8:c.2976-2A>T MANE Select	ENSP00000260570.3:n.2976-2A>T
NM_015662.2:c.2976-2A>T	NP_056477.1:n.2976-2A>T
ENST00000260570.7:c.2976-2A>T	ENSP00000260570.3:n.2976-2A>T
ENST00000476693.1:n.434-2A>T
ENST00000507184.5:n.3255A>T
ENST00000674701.1:c.*2296A>T	ENSP00000502275.1:n.*2296A>T
ENST00000674824.1:c.*991-2A>T	ENSP00000501824.1:n.*991-2A>T
ENST00000674932.1:c.*3229A>T	ENSP00000501967.1:n.*3229A>T
ENST00000675410.1:c.*656-2A>T	ENSP00000502030.1:n.*656-2A>T
ENST00000675690.1:c.2910-2A>T	ENSP00000502283.1:n.2910-2A>T
ENST00000676119.1:c.*2266-2A>T	ENSP00000501701.1:n.*2266-2A>T
XM_005264254.1:c.2910-2A>T	XP_005264311.1:n.2910-2A>T
XM_006711986.2:c.2913-2A>T	XP_006712049.1:n.2913-2A>T
XM_006711986.3:c.2913-2A>T	XP_006712049.1:n.2913-2A>T
XM_006711987.1:c.2976-2A>T	XP_006712050.1:n.2976-2A>T
XM_011532757.1:c.2295-2A>T	XP_011531059.1:n.2295-2A>T
XM_011532757.2:c.2295-2A>T	XP_011531059.1:n.2295-2A>T
XM_011532758.1:c.2976-2A>T	XP_011531060.1:n.2976-2A>T
XM_011532759.1:c.1416-2A>T	XP_011531061.1:n.1416-2A>T
XM_011532759.2:c.1416-2A>T	XP_011531061.1:n.1416-2A>T
XM_011532760.1:c.1041-2A>T	XP_011531062.1:n.1041-2A>T
XM_011532760.2:c.1041-2A>T	XP_011531062.1:n.1041-2A>T
XM_017003790.1:c.2847-2A>T	XP_016859279.1:n.2847-2A>T
XM_017003791.1:c.2295-2A>T	XP_016859280.1:n.2295-2A>T
XM_017003792.1:c.2976-2A>T	XP_016859281.1:n.2976-2A>T
XM_017003793.1:c.1113-2A>T	XP_016859282.1:n.1113-2A>T
XM_017003794.1:c.1113-2A>T	XP_016859283.1:n.1113-2A>T
XM_017003795.1:c.909-2A>T	XP_016859284.1:n.909-2A>T
XR_001738698.1:n.3031-2A>T