Canonical Allele Identifier: CA425415285

Gene: IFT172

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27485041A>G , CM000664.2:g.27485041A>G	GRCh38
NC_000002.11:g.27707908A>G , CM000664.1:g.27707908A>G	GRCh37
NC_000002.10:g.27561412A>G	NCBI36
NG_034068.1:g.9771T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015662.3:c.273T>C MANE Select	NP_056477.1:p.Tyr91=
ENST00000260570.8:c.273T>C MANE Select	ENSP00000260570.3:p.Tyr91=
NM_015662.2:c.273T>C	NP_056477.1:p.Tyr91=
ENST00000260570.7:c.273T>C	ENSP00000260570.3:p.Tyr91=
ENST00000359466.10:c.273T>C	ENSP00000352443.6:p.Tyr91=
ENST00000416524.2:c.210T>C	ENSP00000407408.2:p.Tyr70=
ENST00000475476.2:n.374T>C
ENST00000476264.6:n.353T>C
ENST00000476264.7:n.363T>C
ENST00000507184.5:n.405T>C
ENST00000511842.5:n.298T>C
ENST00000674701.1:c.273T>C	ENSP00000502275.1:p.Tyr91=
ENST00000674824.1:c.210T>C	ENSP00000501824.1:p.Tyr70=
ENST00000674932.1:c.273T>C	ENSP00000501967.1:p.Tyr91=
ENST00000675410.1:c.-385-775T>C	ENSP00000502030.1:n.-385-775T>C
ENST00000675618.1:n.353T>C
ENST00000675690.1:c.273T>C	ENSP00000502283.1:p.Tyr91=
ENST00000675728.1:c.210T>C	ENSP00000501700.1:p.Tyr70=
ENST00000675729.1:c.273T>C	ENSP00000502319.1:p.Tyr91=
ENST00000675757.1:n.158T>C
ENST00000675925.1:n.654T>C
ENST00000675963.1:c.273T>C	ENSP00000502708.1:p.Tyr91=
ENST00000676119.1:c.273T>C	ENSP00000501701.1:p.Tyr91=
ENST00000676300.1:n.359T>C
XM_005264254.1:c.273T>C	XP_005264311.1:p.Tyr91=
XM_006711986.2:c.210T>C	XP_006712049.1:p.Tyr70=
XM_006711986.3:c.210T>C	XP_006712049.1:p.Tyr70=
XM_006711987.1:c.273T>C	XP_006712050.1:p.Tyr91=
XM_011532757.2:c.-608T>C	XP_011531059.1:n.-608T>C
XM_011532758.1:c.273T>C	XP_011531060.1:p.Tyr91=
XM_017003790.1:c.210T>C	XP_016859279.1:p.Tyr70=
XM_017003791.1:c.-369T>C	XP_016859280.1:n.-369T>C
XM_017003792.1:c.273T>C	XP_016859281.1:p.Tyr91=
XM_017003793.1:c.-1138T>C	XP_016859282.1:n.-1138T>C
XM_017003795.1:c.-1749T>C	XP_016859284.1:n.-1749T>C
XR_001738698.1:n.328T>C