Canonical Allele Identifier: CA346397006

Gene: IFT172

Linked Data

• dbSNP Id: rs1668249577
• MyVariant Identifiers: chr2:g.27702931C>T (hg19) ; chr2:g.27480064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27480064C>T , CM000664.2:g.27480064C>T	GRCh38
NC_000002.11:g.27702931C>T , CM000664.1:g.27702931C>T	GRCh37
NC_000002.10:g.27556435C>T	NCBI36
NG_034068.1:g.14748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.871G>A MANE Select	ENSP00000260570.3:p.Ala291Thr
ENST00000476264.7:n.1160G>A
ENST00000674701.1:c.871G>A	ENSP00000502275.1:p.Ala291Thr
ENST00000674824.1:c.808G>A	ENSP00000501824.1:p.Ala270Thr
ENST00000674932.1:c.*534G>A	ENSP00000501967.1:n.*534G>A
ENST00000675410.1:c.190G>A	ENSP00000502030.1:p.Ala64Thr
ENST00000675618.1:n.951G>A
ENST00000675690.1:c.871G>A	ENSP00000502283.1:p.Ala291Thr
ENST00000675728.1:c.808G>A	ENSP00000501700.1:p.Ala270Thr
ENST00000675729.1:c.871G>A	ENSP00000502319.1:p.Ala291Thr
ENST00000675963.1:c.*569G>A	ENSP00000502708.1:n.*569G>A
ENST00000676119.1:c.*161G>A	ENSP00000501701.1:n.*161G>A
ENST00000676300.1:n.957G>A
ENST00000260570.7:c.871G>A	ENSP00000260570.3:p.Ala291Thr
ENST00000359466.10:c.871G>A	ENSP00000352443.6:p.Ala291Thr
ENST00000416524.2:c.808G>A	ENSP00000407408.2:p.Ala270Thr
ENST00000476264.6:n.817G>A
ENST00000507184.5:n.1003G>A
ENST00000511842.5:n.896G>A
NM_015662.2:c.871G>A	NP_056477.1:p.Ala291Thr
XM_005264254.1:c.871G>A	XP_005264311.1:p.Ala291Thr
XM_006711986.2:c.808G>A	XP_006712049.1:p.Ala270Thr
XM_006711987.1:c.871G>A	XP_006712050.1:p.Ala291Thr
XM_011532757.1:c.190G>A	XP_011531059.1:p.Ala64Thr
XM_011532758.1:c.871G>A	XP_011531060.1:p.Ala291Thr
XM_006711986.3:c.808G>A	XP_006712049.1:p.Ala270Thr
XM_011532757.2:c.190G>A	XP_011531059.1:p.Ala64Thr
XM_017003790.1:c.808G>A	XP_016859279.1:p.Ala270Thr
XM_017003791.1:c.190G>A	XP_016859280.1:p.Ala64Thr
XM_017003792.1:c.871G>A	XP_016859281.1:p.Ala291Thr
XM_017003793.1:c.-580G>A	XP_016859282.1:n.-580G>A
XM_017003794.1:c.-580G>A	XP_016859283.1:n.-580G>A
XM_017003795.1:c.-952G>A	XP_016859284.1:n.-952G>A
XR_001738698.1:n.926G>A
NM_015662.3:c.871G>A MANE Select	NP_056477.1:p.Ala291Thr