Canonical Allele Identifier: CA394201396

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1558135C>G , CM000678.2:g.1558135C>G	GRCh38
NC_000016.9:g.1608136C>G , CM000678.1:g.1608136C>G	GRCh37
NC_000016.8:g.1548137C>G	NCBI36
NG_032783.1:g.58974G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.2200-1G>C MANE Select	NP_055529.2:n.2200-1G>C
ENST00000426508.7:c.2200-1G>C MANE Select	ENSP00000406012.2:n.2200-1G>C
NM_014714.3:c.2200-1G>C	NP_055529.2:n.2200-1G>C
ENST00000397417.6:c.*752-1G>C	ENSP00000380562.2:n.*752-1G>C
ENST00000426508.6:c.2200-1G>C	ENSP00000406012.2:n.2200-1G>C
ENST00000439987.6:n.2261-1G>C
ENST00000561954.1:n.247-1G>C
ENST00000565298.5:n.888-1G>C
XM_005255725.3:c.2200-1G>C	XP_005255782.1:n.2200-1G>C
XM_005255725.5:c.2200-1G>C	XP_005255782.1:n.2200-1G>C
XM_005255726.2:c.2200-1G>C	XP_005255783.1:n.2200-1G>C
XM_005255726.4:c.2200-1G>C	XP_005255783.1:n.2200-1G>C
XM_006720989.2:c.2200-1G>C	XP_006721052.1:n.2200-1G>C
XM_006720990.2:c.2200-1G>C	XP_006721053.1:n.2200-1G>C
XM_006720990.3:c.2200-1G>C	XP_006721053.1:n.2200-1G>C
XM_006720991.2:c.2200-1G>C	XP_006721054.1:n.2200-1G>C
XM_006720991.3:c.2200-1G>C	XP_006721054.1:n.2200-1G>C
XM_011522766.1:c.1954-1G>C	XP_011521068.1:n.1954-1G>C
XM_011522766.3:c.1954-1G>C	XP_011521068.1:n.1954-1G>C
XM_011522767.1:c.1225-1G>C	XP_011521069.1:n.1225-1G>C
XM_011522767.2:c.1225-1G>C	XP_011521069.1:n.1225-1G>C
XM_011522768.1:c.2200-1G>C	XP_011521070.1:n.2200-1G>C
XM_011522769.1:c.2200-1G>C	XP_011521071.1:n.2200-1G>C
XM_011522769.3:c.2200-1G>C	XP_011521071.1:n.2200-1G>C
XM_011522771.1:c.2200-1G>C	XP_011521073.1:n.2200-1G>C
XM_011522771.3:c.2200-1G>C	XP_011521073.1:n.2200-1G>C
XM_011522772.1:c.2200-1G>C	XP_011521074.1:n.2200-1G>C
XM_011522772.3:c.2200-1G>C	XP_011521074.1:n.2200-1G>C
XM_017023910.1:c.2200-1G>C	XP_016879399.1:n.2200-1G>C
XM_017023911.1:c.385-1G>C	XP_016879400.1:n.385-1G>C