Canonical Allele Identifier: CA394225442

Gene: IFT140

Linked Data

• gnomAD v4: 16-1523661-T-G
• MyVariant Identifiers: chr16:g.1573662T>G (hg19) ; chr16:g.1523661T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523661T>G , CM000678.2:g.1523661T>G	GRCh38
NC_000016.9:g.1573662T>G , CM000678.1:g.1573662T>G	GRCh37
NC_000016.8:g.1513663T>G	NCBI36
NG_032783.1:g.93448A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3310A>C MANE Select	ENSP00000406012.2:p.Thr1104Pro
ENST00000361339.9:c.892A>C	ENSP00000354895.5:p.Thr298Pro
ENST00000397417.6:c.*1748A>C	ENSP00000380562.2:n.*1748A>C
ENST00000426508.6:c.3310A>C	ENSP00000406012.2:p.Thr1104Pro
ENST00000565298.5:n.3134A>C
NM_014714.3:c.3310A>C	NP_055529.2:p.Thr1104Pro
XM_006720989.2:c.3310A>C	XP_006721052.1:p.Thr1104Pro
XM_006720990.2:c.3310A>C	XP_006721053.1:p.Thr1104Pro
XM_006720991.2:c.3310A>C	XP_006721054.1:p.Thr1104Pro
XM_006720992.2:c.943A>C	XP_006721055.1:p.Thr315Pro
XM_011522766.1:c.3064A>C	XP_011521068.1:p.Thr1022Pro
XM_011522767.1:c.2335A>C	XP_011521069.1:p.Thr779Pro
XM_006720990.3:c.3310A>C	XP_006721053.1:p.Thr1104Pro
XM_006720991.3:c.3310A>C	XP_006721054.1:p.Thr1104Pro
XM_006720992.3:c.943A>C	XP_006721055.1:p.Thr315Pro
XM_011522766.3:c.3064A>C	XP_011521068.1:p.Thr1022Pro
XM_011522767.2:c.2335A>C	XP_011521069.1:p.Thr779Pro
XM_017023910.1:c.3310A>C	XP_016879399.1:p.Thr1104Pro
XM_017023911.1:c.1495A>C	XP_016879400.1:p.Thr499Pro
NM_014714.4:c.3310A>C MANE Select	NP_055529.2:p.Thr1104Pro