Canonical Allele Identifier: CA2201723404

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520096_1520097delinsCG , CM000678.2:g.1520096_1520097delinsCG	GRCh38
NC_000016.9:g.1570097_1570098delinsCG , CM000678.1:g.1570097_1570098delinsCG	GRCh37
NC_000016.8:g.1510098_1510099delinsCG	NCBI36
NG_032783.1:g.97012_97013delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3873+34_3873+35delinsCG MANE Select	ENSP00000406012.2:n.3873+34_3873+35delinsCG
ENST00000361339.9:c.1455+34_1455+35delinsCG	ENSP00000354895.5:n.1455+34_1455+35delinsCG
ENST00000397417.6:c.*2311+34_*2311+35delinsCG	ENSP00000380562.2:n.*2311+34_*2311+35delinsCG
ENST00000426508.6:c.3873+34_3873+35delinsCG	ENSP00000406012.2:n.3873+34_3873+35delinsCG
ENST00000565298.5:n.3697+34_3697+35delinsCG
NM_014714.3:c.3873+34_3873+35delinsCG	NP_055529.2:n.3873+34_3873+35delinsCG
XM_006720989.2:c.3873+34_3873+35delinsCG	XP_006721052.1:n.3873+34_3873+35delinsCG
XM_006720990.2:c.3873+34_3873+35delinsCG	XP_006721053.1:n.3873+34_3873+35delinsCG
XM_006720991.2:c.3873+34_3873+35delinsCG	XP_006721054.1:n.3873+34_3873+35delinsCG
XM_006720992.2:c.1506+34_1506+35delinsCG	XP_006721055.1:n.1506+34_1506+35delinsCG
XM_011522766.1:c.3627+34_3627+35delinsCG	XP_011521068.1:n.3627+34_3627+35delinsCG
XM_011522767.1:c.2898+34_2898+35delinsCG	XP_011521069.1:n.2898+34_2898+35delinsCG
XM_006720990.3:c.3873+34_3873+35delinsCG	XP_006721053.1:n.3873+34_3873+35delinsCG
XM_006720991.3:c.3873+34_3873+35delinsCG	XP_006721054.1:n.3873+34_3873+35delinsCG
XM_006720992.3:c.1506+34_1506+35delinsCG	XP_006721055.1:n.1506+34_1506+35delinsCG
XM_011522766.3:c.3627+34_3627+35delinsCG	XP_011521068.1:n.3627+34_3627+35delinsCG
XM_011522767.2:c.2898+34_2898+35delinsCG	XP_011521069.1:n.2898+34_2898+35delinsCG
XM_017023910.1:c.3873+34_3873+35delinsCG	XP_016879399.1:n.3873+34_3873+35delinsCG
XM_017023911.1:c.2058+34_2058+35delinsCG	XP_016879400.1:n.2058+34_2058+35delinsCG
NM_014714.4:c.3873+34_3873+35delinsCG MANE Select	NP_055529.2:n.3873+34_3873+35delinsCG