Canonical Allele Identifier: CA425413797
Gene: IFT172 HGNC NCBI

Linked Data

gnomAD v4: 2-27480041-G-C
MyVariant Identifiers: chr2:g.27702908G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27480041G>C , CM000664.2:g.27480041G>C GRCh38
NC_000002.11:g.27702908G>C , CM000664.1:g.27702908G>C GRCh37
NC_000002.10:g.27556412G>C NCBI36
NG_034068.1:g.14771C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260570.8:c.894C>G MANE Select ENSP00000260570.3:p.Gly298=
ENST00000476264.7:n.1183C>G
ENST00000674701.1:c.894C>G ENSP00000502275.1:p.Gly298=
ENST00000674824.1:c.831C>G ENSP00000501824.1:p.Gly277=
ENST00000674932.1:c.*557C>G ENSP00000501967.1:n.*557C>G
ENST00000675410.1:c.213C>G ENSP00000502030.1:p.Gly71=
ENST00000675618.1:n.974C>G
ENST00000675690.1:c.894C>G ENSP00000502283.1:p.Gly298=
ENST00000675728.1:c.831C>G ENSP00000501700.1:p.Gly277=
ENST00000675729.1:c.894C>G ENSP00000502319.1:p.Gly298=
ENST00000675963.1:c.*592C>G ENSP00000502708.1:n.*592C>G
ENST00000676119.1:c.*184C>G ENSP00000501701.1:n.*184C>G
ENST00000676300.1:n.980C>G
ENST00000260570.7:c.894C>G ENSP00000260570.3:p.Gly298=
ENST00000359466.10:c.894C>G ENSP00000352443.6:p.Gly298=
ENST00000416524.2:c.831C>G ENSP00000407408.2:p.Gly277=
ENST00000476264.6:n.840C>G
ENST00000507184.5:n.1026C>G
ENST00000511842.5:n.919C>G
NM_015662.2:c.894C>G NP_056477.1:p.Gly298=
XM_005264254.1:c.894C>G XP_005264311.1:p.Gly298=
XM_006711986.2:c.831C>G XP_006712049.1:p.Gly277=
XM_006711987.1:c.894C>G XP_006712050.1:p.Gly298=
XM_011532757.1:c.213C>G XP_011531059.1:p.Gly71=
XM_011532758.1:c.894C>G XP_011531060.1:p.Gly298=
XM_006711986.3:c.831C>G XP_006712049.1:p.Gly277=
XM_011532757.2:c.213C>G XP_011531059.1:p.Gly71=
XM_017003790.1:c.831C>G XP_016859279.1:p.Gly277=
XM_017003791.1:c.213C>G XP_016859280.1:p.Gly71=
XM_017003792.1:c.894C>G XP_016859281.1:p.Gly298=
XM_017003793.1:c.-557C>G XP_016859282.1:n.-557C>G
XM_017003794.1:c.-557C>G XP_016859283.1:n.-557C>G
XM_017003795.1:c.-929C>G XP_016859284.1:n.-929C>G
XR_001738698.1:n.949C>G
NM_015662.3:c.894C>G MANE Select NP_056477.1:p.Gly298=