Canonical Allele Identifier: CA2201723388
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520074T= , CM000678.2:g.1520074T= GRCh38
NC_000016.9:g.1570075T= , CM000678.1:g.1570075T= GRCh37
NC_000016.8:g.1510076T= NCBI36
NG_032783.1:g.97035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3874-27A= MANE Select ENSP00000406012.2:n.3874-27A=
ENST00000361339.9:c.1456-27A= ENSP00000354895.5:n.1456-27A=
ENST00000397417.6:c.*2312-27A= ENSP00000380562.2:n.*2312-27A=
ENST00000426508.6:c.3874-27A= ENSP00000406012.2:n.3874-27A=
ENST00000565298.5:n.3698-27A=
NM_014714.3:c.3874-27A= NP_055529.2:n.3874-27A=
XM_006720989.2:c.3874-27A= XP_006721052.1:n.3874-27A=
XM_006720990.2:c.3874-27A= XP_006721053.1:n.3874-27A=
XM_006720991.2:c.3874-27A= XP_006721054.1:n.3874-27A=
XM_006720992.2:c.1507-27A= XP_006721055.1:n.1507-27A=
XM_011522766.1:c.3628-27A= XP_011521068.1:n.3628-27A=
XM_011522767.1:c.2899-27A= XP_011521069.1:n.2899-27A=
XM_006720990.3:c.3874-27A= XP_006721053.1:n.3874-27A=
XM_006720991.3:c.3874-27A= XP_006721054.1:n.3874-27A=
XM_006720992.3:c.1507-27A= XP_006721055.1:n.1507-27A=
XM_011522766.3:c.3628-27A= XP_011521068.1:n.3628-27A=
XM_011522767.2:c.2899-27A= XP_011521069.1:n.2899-27A=
XM_017023910.1:c.3874-27A= XP_016879399.1:n.3874-27A=
XM_017023911.1:c.2059-27A= XP_016879400.1:n.2059-27A=
NM_014714.4:c.3874-27A= MANE Select NP_055529.2:n.3874-27A=