Canonical Allele Identifier: CA493031389

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1561014G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511013G>C , CM000678.2:g.1511013G>C	GRCh38
NC_000016.9:g.1561014G>C , CM000678.1:g.1561014G>C	GRCh37
NC_000016.8:g.1501015G>C	NCBI36
NG_032783.1:g.106096C>G
NG_050910.1:g.22670G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4320C>G MANE Select	ENSP00000406012.2:p.Arg1440=
ENST00000361339.9:c.1902C>G	ENSP00000354895.5:p.Arg634=
ENST00000397417.6:c.*2758C>G	ENSP00000380562.2:n.*2758C>G
ENST00000426508.6:c.4320C>G	ENSP00000406012.2:p.Arg1440=
ENST00000565298.5:n.4144C>G
NM_014714.3:c.4320C>G	NP_055529.2:p.Arg1440=
XM_006720989.2:c.4320C>G	XP_006721052.1:p.Arg1440=
XM_006720990.2:c.4320C>G	XP_006721053.1:p.Arg1440=
XM_006720991.2:c.4320C>G	XP_006721054.1:p.Arg1440=
XM_006720992.2:c.1953C>G	XP_006721055.1:p.Arg651=
XM_011522766.1:c.4074C>G	XP_011521068.1:p.Arg1358=
XM_011522767.1:c.3345C>G	XP_011521069.1:p.Arg1115=
XM_006720990.3:c.4320C>G	XP_006721053.1:p.Arg1440=
XM_006720991.3:c.4320C>G	XP_006721054.1:p.Arg1440=
XM_006720992.3:c.1953C>G	XP_006721055.1:p.Arg651=
XM_011522766.3:c.4074C>G	XP_011521068.1:p.Arg1358=
XM_011522767.2:c.3345C>G	XP_011521069.1:p.Arg1115=
XM_017023910.1:c.4320C>G	XP_016879399.1:p.Arg1440=
XM_017023911.1:c.2505C>G	XP_016879400.1:p.Arg835=
NM_014714.4:c.4320C>G MANE Select	NP_055529.2:p.Arg1440=