Canonical Allele Identifier: CA2201699084

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525884_1525888delinsCACTA , CM000678.2:g.1525884_1525888delinsCACTA	GRCh38
NC_000016.9:g.1575885_1575889delinsCACTA , CM000678.1:g.1575885_1575889delinsCACTA	GRCh37
NC_000016.8:g.1515886_1515890delinsCACTA	NCBI36
NG_032783.1:g.91221_91225delinsTAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2767_2768+3delinsTAGTG
ENST00000361339.9:c.349_350+3delinsTAGTG
ENST00000397417.6:c.*1205_*1206+3delinsTAGTG
ENST00000426508.6:c.2767_2768+3delinsTAGTG
ENST00000565298.5:n.1996_1997+3delinsTAGTG
ENST00000566818.1:n.482_483+3delinsTAGTG
NM_014714.3:c.2767_2768+3delinsTAGTG
XM_006720989.2:c.2767_2768+3delinsTAGTG
XM_006720990.2:c.2767_2768+3delinsTAGTG
XM_006720991.2:c.2767_2768+3delinsTAGTG
XM_006720992.2:c.400_401+3delinsTAGTG
XM_011522766.1:c.2521_2522+3delinsTAGTG
XM_011522767.1:c.1792_1793+3delinsTAGTG
XM_006720990.3:c.2767_2768+3delinsTAGTG
XM_006720991.3:c.2767_2768+3delinsTAGTG
XM_006720992.3:c.400_401+3delinsTAGTG
XM_011522766.3:c.2521_2522+3delinsTAGTG
XM_011522767.2:c.1792_1793+3delinsTAGTG
XM_017023910.1:c.2767_2768+3delinsTAGTG
XM_017023911.1:c.952_953+3delinsTAGTG
NM_014714.4:c.2767_2768+3delinsTAGTG