Canonical Allele Identifier: CA1580647

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27472348C>T , CM000664.2:g.27472348C>T	GRCh38
NC_000002.11:g.27695215C>T , CM000664.1:g.27695215C>T	GRCh37
NC_000002.10:g.27548719C>T	NCBI36
NG_034068.1:g.22464G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015662.3:c.1426G>A MANE Select	NP_056477.1:p.Gly476Ser
ENST00000260570.8:c.1426G>A MANE Select	ENSP00000260570.3:p.Gly476Ser
NM_015662.2:c.1426G>A	NP_056477.1:p.Gly476Ser
ENST00000260570.7:c.1426G>A	ENSP00000260570.3:p.Gly476Ser
ENST00000359466.10:c.1426G>A	ENSP00000352443.6:p.Gly476Ser
ENST00000416524.2:c.1363G>A	ENSP00000407408.2:p.Gly455Ser
ENST00000476264.6:n.1862G>A
ENST00000507184.5:n.1558G>A
ENST00000511842.5:n.1451G>A
ENST00000674701.1:c.1426G>A	ENSP00000502275.1:p.Gly476Ser
ENST00000674824.1:c.1363G>A	ENSP00000501824.1:p.Gly455Ser
ENST00000674932.1:c.*1089G>A	ENSP00000501967.1:n.*1089G>A
ENST00000675410.1:c.745G>A	ENSP00000502030.1:p.Gly249Ser
ENST00000675618.1:n.1996G>A
ENST00000675690.1:c.1426G>A	ENSP00000502283.1:p.Gly476Ser
ENST00000675728.1:c.1363G>A	ENSP00000501700.1:p.Gly455Ser
ENST00000675729.1:c.1340G>A	ENSP00000502319.1:p.Trp447Ter
ENST00000675963.1:c.*1124G>A	ENSP00000502708.1:n.*1124G>A
ENST00000676119.1:c.*716G>A	ENSP00000501701.1:n.*716G>A
XM_005264254.1:c.1426G>A	XP_005264311.1:p.Gly476Ser
XM_006711986.2:c.1363G>A	XP_006712049.1:p.Gly455Ser
XM_006711986.3:c.1363G>A	XP_006712049.1:p.Gly455Ser
XM_006711987.1:c.1426G>A	XP_006712050.1:p.Gly476Ser
XM_011532757.1:c.745G>A	XP_011531059.1:p.Gly249Ser
XM_011532757.2:c.745G>A	XP_011531059.1:p.Gly249Ser
XM_011532758.1:c.1426G>A	XP_011531060.1:p.Gly476Ser
XM_017003790.1:c.1363G>A	XP_016859279.1:p.Gly455Ser
XM_017003791.1:c.745G>A	XP_016859280.1:p.Gly249Ser
XM_017003792.1:c.1426G>A	XP_016859281.1:p.Gly476Ser
XM_017003793.1:c.-25G>A	XP_016859282.1:n.-25G>A
XM_017003794.1:c.-25G>A	XP_016859283.1:n.-25G>A
XM_017003795.1:c.-397G>A	XP_016859284.1:n.-397G>A
XR_001738698.1:n.1481G>A