Canonical Allele Identifier: CA346397478

Gene: IFT172

Linked Data

• MyVariant Identifiers: chr2:g.27703006A>T (hg19) ; chr2:g.27480139A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27480139A>T , CM000664.2:g.27480139A>T	GRCh38
NC_000002.11:g.27703006A>T , CM000664.1:g.27703006A>T	GRCh37
NC_000002.10:g.27556510A>T	NCBI36
NG_034068.1:g.14673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260570.8:c.796T>A MANE Select	ENSP00000260570.3:p.Phe266Ile
ENST00000476264.7:n.1085T>A
ENST00000674701.1:c.796T>A	ENSP00000502275.1:p.Phe266Ile
ENST00000674824.1:c.733T>A	ENSP00000501824.1:p.Phe245Ile
ENST00000674932.1:c.*459T>A	ENSP00000501967.1:n.*459T>A
ENST00000675410.1:c.115T>A	ENSP00000502030.1:p.Phe39Ile
ENST00000675618.1:n.876T>A
ENST00000675690.1:c.796T>A	ENSP00000502283.1:p.Phe266Ile
ENST00000675728.1:c.733T>A	ENSP00000501700.1:p.Phe245Ile
ENST00000675729.1:c.796T>A	ENSP00000502319.1:p.Phe266Ile
ENST00000675963.1:c.*494T>A	ENSP00000502708.1:n.*494T>A
ENST00000676119.1:c.*86T>A	ENSP00000501701.1:n.*86T>A
ENST00000676300.1:n.882T>A
ENST00000260570.7:c.796T>A	ENSP00000260570.3:p.Phe266Ile
ENST00000359466.10:c.796T>A	ENSP00000352443.6:p.Phe266Ile
ENST00000416524.2:c.733T>A	ENSP00000407408.2:p.Phe245Ile
ENST00000476264.6:n.742T>A
ENST00000507184.5:n.928T>A
ENST00000511842.5:n.821T>A
NM_015662.2:c.796T>A	NP_056477.1:p.Phe266Ile
XM_005264254.1:c.796T>A	XP_005264311.1:p.Phe266Ile
XM_006711986.2:c.733T>A	XP_006712049.1:p.Phe245Ile
XM_006711987.1:c.796T>A	XP_006712050.1:p.Phe266Ile
XM_011532757.1:c.115T>A	XP_011531059.1:p.Phe39Ile
XM_011532758.1:c.796T>A	XP_011531060.1:p.Phe266Ile
XM_006711986.3:c.733T>A	XP_006712049.1:p.Phe245Ile
XM_011532757.2:c.115T>A	XP_011531059.1:p.Phe39Ile
XM_017003790.1:c.733T>A	XP_016859279.1:p.Phe245Ile
XM_017003791.1:c.115T>A	XP_016859280.1:p.Phe39Ile
XM_017003792.1:c.796T>A	XP_016859281.1:p.Phe266Ile
XM_017003793.1:c.-655T>A	XP_016859282.1:n.-655T>A
XM_017003794.1:c.-655T>A	XP_016859283.1:n.-655T>A
XM_017003795.1:c.-1027T>A	XP_016859284.1:n.-1027T>A
XR_001738698.1:n.851T>A
NM_015662.3:c.796T>A MANE Select	NP_056477.1:p.Phe266Ile