Canonical Allele Identifier: CA7812831

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511128A>G , CM000678.2:g.1511128A>G	GRCh38
NC_000016.9:g.1561129A>G , CM000678.1:g.1561129A>G	GRCh37
NC_000016.8:g.1501130A>G	NCBI36
NG_032783.1:g.105981T>C
NG_050910.1:g.22785A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.4205T>C MANE Select	NP_055529.2:p.Met1402Thr
ENST00000426508.7:c.4205T>C MANE Select	ENSP00000406012.2:p.Met1402Thr
NM_014714.3:c.4205T>C	NP_055529.2:p.Met1402Thr
ENST00000361339.9:c.1787T>C	ENSP00000354895.5:p.Met596Thr
ENST00000397417.6:c.*2643T>C	ENSP00000380562.2:n.*2643T>C
ENST00000426508.6:c.4205T>C	ENSP00000406012.2:p.Met1402Thr
ENST00000565298.5:n.4029T>C
XM_006720989.2:c.4205T>C	XP_006721052.1:p.Met1402Thr
XM_006720990.2:c.4205T>C	XP_006721053.1:p.Met1402Thr
XM_006720990.3:c.4205T>C	XP_006721053.1:p.Met1402Thr
XM_006720991.2:c.4205T>C	XP_006721054.1:p.Met1402Thr
XM_006720991.3:c.4205T>C	XP_006721054.1:p.Met1402Thr
XM_006720992.2:c.1838T>C	XP_006721055.1:p.Met613Thr
XM_006720992.3:c.1838T>C	XP_006721055.1:p.Met613Thr
XM_011522766.1:c.3959T>C	XP_011521068.1:p.Met1320Thr
XM_011522766.3:c.3959T>C	XP_011521068.1:p.Met1320Thr
XM_011522767.1:c.3230T>C	XP_011521069.1:p.Met1077Thr
XM_011522767.2:c.3230T>C	XP_011521069.1:p.Met1077Thr
XM_017023910.1:c.4205T>C	XP_016879399.1:p.Met1402Thr
XM_017023911.1:c.2390T>C	XP_016879400.1:p.Met797Thr