Canonical Allele Identifier: CA394228426

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1526753G>A , CM000678.2:g.1526753G>A	GRCh38
NC_000016.9:g.1576754G>A , CM000678.1:g.1576754G>A	GRCh37
NC_000016.8:g.1516755G>A	NCBI36
NG_032783.1:g.90356C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.2443C>T MANE Select	NP_055529.2:p.Gln815Ter
ENST00000426508.7:c.2443C>T MANE Select	ENSP00000406012.2:p.Gln815Ter
NM_014714.3:c.2443C>T	NP_055529.2:p.Gln815Ter
ENST00000361339.9:c.25C>T	ENSP00000354895.5:p.Gln9Ter
ENST00000397417.6:c.*995C>T	ENSP00000380562.2:n.*995C>T
ENST00000426508.6:c.2443C>T	ENSP00000406012.2:p.Gln815Ter
ENST00000565298.5:n.1131C>T
ENST00000566818.1:n.272C>T
XM_006720989.2:c.2443C>T	XP_006721052.1:p.Gln815Ter
XM_006720990.2:c.2443C>T	XP_006721053.1:p.Gln815Ter
XM_006720990.3:c.2443C>T	XP_006721053.1:p.Gln815Ter
XM_006720991.2:c.2443C>T	XP_006721054.1:p.Gln815Ter
XM_006720991.3:c.2443C>T	XP_006721054.1:p.Gln815Ter
XM_006720992.2:c.76C>T	XP_006721055.1:p.Gln26Ter
XM_006720992.3:c.76C>T	XP_006721055.1:p.Gln26Ter
XM_011522766.1:c.2197C>T	XP_011521068.1:p.Gln733Ter
XM_011522766.3:c.2197C>T	XP_011521068.1:p.Gln733Ter
XM_011522767.1:c.1468C>T	XP_011521069.1:p.Gln490Ter
XM_011522767.2:c.1468C>T	XP_011521069.1:p.Gln490Ter
XM_017023910.1:c.2443C>T	XP_016879399.1:p.Gln815Ter
XM_017023911.1:c.628C>T	XP_016879400.1:p.Gln210Ter