Canonical Allele Identifier: CA493031422

Gene: IFT140

Linked Data

• gnomAD v4: 16-1511034-G-A
• MyVariant Identifiers: chr16:g.1561035G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511034G>A , CM000678.2:g.1511034G>A	GRCh38
NC_000016.9:g.1561035G>A , CM000678.1:g.1561035G>A	GRCh37
NC_000016.8:g.1501036G>A	NCBI36
NG_032783.1:g.106075C>T
NG_050910.1:g.22691G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4299C>T MANE Select	ENSP00000406012.2:p.Arg1433=
ENST00000361339.9:c.1881C>T	ENSP00000354895.5:p.Arg627=
ENST00000397417.6:c.*2737C>T	ENSP00000380562.2:n.*2737C>T
ENST00000426508.6:c.4299C>T	ENSP00000406012.2:p.Arg1433=
ENST00000565298.5:n.4123C>T
NM_014714.3:c.4299C>T	NP_055529.2:p.Arg1433=
XM_006720989.2:c.4299C>T	XP_006721052.1:p.Arg1433=
XM_006720990.2:c.4299C>T	XP_006721053.1:p.Arg1433=
XM_006720991.2:c.4299C>T	XP_006721054.1:p.Arg1433=
XM_006720992.2:c.1932C>T	XP_006721055.1:p.Arg644=
XM_011522766.1:c.4053C>T	XP_011521068.1:p.Arg1351=
XM_011522767.1:c.3324C>T	XP_011521069.1:p.Arg1108=
XM_006720990.3:c.4299C>T	XP_006721053.1:p.Arg1433=
XM_006720991.3:c.4299C>T	XP_006721054.1:p.Arg1433=
XM_006720992.3:c.1932C>T	XP_006721055.1:p.Arg644=
XM_011522766.3:c.4053C>T	XP_011521068.1:p.Arg1351=
XM_011522767.2:c.3324C>T	XP_011521069.1:p.Arg1108=
XM_017023910.1:c.4299C>T	XP_016879399.1:p.Arg1433=
XM_017023911.1:c.2484C>T	XP_016879400.1:p.Arg828=
NM_014714.4:c.4299C>T MANE Select	NP_055529.2:p.Arg1433=