Canonical Allele Identifier: CA394222490

Gene: IFT140

Linked Data

• gnomAD v4: 16-1511100-C-G
• MyVariant Identifiers: chr16:g.1561101C>G (hg19) ; chr16:g.1511100C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511100C>G , CM000678.2:g.1511100C>G	GRCh38
NC_000016.9:g.1561101C>G , CM000678.1:g.1561101C>G	GRCh37
NC_000016.8:g.1501102C>G	NCBI36
NG_032783.1:g.106009G>C
NG_050910.1:g.22757C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4233G>C MANE Select	ENSP00000406012.2:p.Met1411Ile
ENST00000361339.9:c.1815G>C	ENSP00000354895.5:p.Met605Ile
ENST00000397417.6:c.*2671G>C	ENSP00000380562.2:n.*2671G>C
ENST00000426508.6:c.4233G>C	ENSP00000406012.2:p.Met1411Ile
ENST00000565298.5:n.4057G>C
NM_014714.3:c.4233G>C	NP_055529.2:p.Met1411Ile
XM_006720989.2:c.4233G>C	XP_006721052.1:p.Met1411Ile
XM_006720990.2:c.4233G>C	XP_006721053.1:p.Met1411Ile
XM_006720991.2:c.4233G>C	XP_006721054.1:p.Met1411Ile
XM_006720992.2:c.1866G>C	XP_006721055.1:p.Met622Ile
XM_011522766.1:c.3987G>C	XP_011521068.1:p.Met1329Ile
XM_011522767.1:c.3258G>C	XP_011521069.1:p.Met1086Ile
XM_006720990.3:c.4233G>C	XP_006721053.1:p.Met1411Ile
XM_006720991.3:c.4233G>C	XP_006721054.1:p.Met1411Ile
XM_006720992.3:c.1866G>C	XP_006721055.1:p.Met622Ile
XM_011522766.3:c.3987G>C	XP_011521068.1:p.Met1329Ile
XM_011522767.2:c.3258G>C	XP_011521069.1:p.Met1086Ile
XM_017023910.1:c.4233G>C	XP_016879399.1:p.Met1411Ile
XM_017023911.1:c.2418G>C	XP_016879400.1:p.Met806Ile
NM_014714.4:c.4233G>C MANE Select	NP_055529.2:p.Met1411Ile