Canonical Allele Identifier: CA1580168

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27458799G>A , CM000664.2:g.27458799G>A	GRCh38
NC_000002.11:g.27681666G>A , CM000664.1:g.27681666G>A	GRCh37
NC_000002.10:g.27535170G>A	NCBI36
NG_034068.1:g.36013C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015662.3:c.2857C>T MANE Select	NP_056477.1:p.Arg953Cys
ENST00000260570.8:c.2857C>T MANE Select	ENSP00000260570.3:p.Arg953Cys
NM_015662.2:c.2857C>T	NP_056477.1:p.Arg953Cys
ENST00000260570.7:c.2857C>T	ENSP00000260570.3:p.Arg953Cys
ENST00000476693.1:n.315C>T
ENST00000507184.5:n.2989C>T
ENST00000674701.1:c.*2030C>T	ENSP00000502275.1:n.*2030C>T
ENST00000674824.1:c.*872C>T	ENSP00000501824.1:n.*872C>T
ENST00000674932.1:c.*2963C>T	ENSP00000501967.1:n.*2963C>T
ENST00000675410.1:c.*537C>T	ENSP00000502030.1:n.*537C>T
ENST00000675690.1:c.2791C>T	ENSP00000502283.1:p.Arg931Cys
ENST00000676119.1:c.*2147C>T	ENSP00000501701.1:n.*2147C>T
XM_005264254.1:c.2791C>T	XP_005264311.1:p.Arg931Cys
XM_006711986.2:c.2794C>T	XP_006712049.1:p.Arg932Cys
XM_006711986.3:c.2794C>T	XP_006712049.1:p.Arg932Cys
XM_006711987.1:c.2857C>T	XP_006712050.1:p.Arg953Cys
XM_011532757.1:c.2176C>T	XP_011531059.1:p.Arg726Cys
XM_011532757.2:c.2176C>T	XP_011531059.1:p.Arg726Cys
XM_011532758.1:c.2857C>T	XP_011531060.1:p.Arg953Cys
XM_011532759.1:c.1297C>T	XP_011531061.1:p.Arg433Cys
XM_011532759.2:c.1297C>T	XP_011531061.1:p.Arg433Cys
XM_011532760.1:c.922C>T	XP_011531062.1:p.Arg308Cys
XM_011532760.2:c.922C>T	XP_011531062.1:p.Arg308Cys
XM_017003790.1:c.2728C>T	XP_016859279.1:p.Arg910Cys
XM_017003791.1:c.2176C>T	XP_016859280.1:p.Arg726Cys
XM_017003792.1:c.2857C>T	XP_016859281.1:p.Arg953Cys
XM_017003793.1:c.994C>T	XP_016859282.1:p.Arg332Cys
XM_017003794.1:c.994C>T	XP_016859283.1:p.Arg332Cys
XM_017003795.1:c.790C>T	XP_016859284.1:p.Arg264Cys
XR_001738698.1:n.2912C>T