Canonical Allele Identifier: CA1581042
Community Standard Title: NM_015662.3(IFT172):c.318C>T (p.Cys106=)
Gene: IFT172 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27484245G>A , CM000664.2:g.27484245G>A GRCh38
NC_000002.11:g.27707112G>A , CM000664.1:g.27707112G>A GRCh37
NC_000002.10:g.27560616G>A NCBI36
NG_034068.1:g.10567C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015662.3:c.318C>T MANE Select NP_056477.1:p.Cys106=
ENST00000260570.8:c.318C>T MANE Select ENSP00000260570.3:p.Cys106=
NM_015662.2:c.318C>T NP_056477.1:p.Cys106=
ENST00000260570.7:c.318C>T ENSP00000260570.3:p.Cys106=
ENST00000359466.10:c.318C>T ENSP00000352443.6:p.Cys106=
ENST00000416524.2:c.255C>T ENSP00000407408.2:p.Cys85=
ENST00000475476.2:n.419C>T
ENST00000476264.6:n.398C>T
ENST00000476264.7:n.408C>T
ENST00000507184.5:n.450C>T
ENST00000511842.5:n.343C>T
ENST00000674701.1:c.318C>T ENSP00000502275.1:p.Cys106=
ENST00000674824.1:c.255C>T ENSP00000501824.1:p.Cys85=
ENST00000674932.1:c.297-308C>T ENSP00000501967.1:n.297-308C>T
ENST00000675410.1:c.-364C>T ENSP00000502030.1:n.-364C>T
ENST00000675618.1:n.398C>T
ENST00000675690.1:c.318C>T ENSP00000502283.1:p.Cys106=
ENST00000675728.1:c.255C>T ENSP00000501700.1:p.Cys85=
ENST00000675729.1:c.318C>T ENSP00000502319.1:p.Cys106=
ENST00000675925.1:n.1450C>T
ENST00000675963.1:c.318C>T ENSP00000502708.1:p.Cys106=
ENST00000676119.1:c.318C>T ENSP00000501701.1:p.Cys106=
ENST00000676300.1:n.404C>T
XM_005264254.1:c.318C>T XP_005264311.1:p.Cys106=
XM_006711986.2:c.255C>T XP_006712049.1:p.Cys85=
XM_006711986.3:c.255C>T XP_006712049.1:p.Cys85=
XM_006711987.1:c.318C>T XP_006712050.1:p.Cys106=
XM_011532757.2:c.-563C>T XP_011531059.1:n.-563C>T
XM_011532758.1:c.318C>T XP_011531060.1:p.Cys106=
XM_017003790.1:c.255C>T XP_016859279.1:p.Cys85=
XM_017003791.1:c.-345-308C>T XP_016859280.1:n.-345-308C>T
XM_017003792.1:c.318C>T XP_016859281.1:p.Cys106=
XM_017003793.1:c.-1114-308C>T XP_016859282.1:n.-1114-308C>T
XM_017003795.1:c.-1704C>T XP_016859284.1:n.-1704C>T
XR_001738698.1:n.373C>T