Canonical Allele Identifier: CA394222334

Gene: IFT140

Linked Data

• gnomAD v4: 16-1511018-C-A
• MyVariant Identifiers: chr16:g.1561019C>A (hg19) ; chr16:g.1511018C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511018C>A , CM000678.2:g.1511018C>A	GRCh38
NC_000016.9:g.1561019C>A , CM000678.1:g.1561019C>A	GRCh37
NC_000016.8:g.1501020C>A	NCBI36
NG_032783.1:g.106091G>T
NG_050910.1:g.22675C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4315G>T MANE Select	ENSP00000406012.2:p.Val1439Phe
ENST00000361339.9:c.1897G>T	ENSP00000354895.5:p.Val633Phe
ENST00000397417.6:c.*2753G>T	ENSP00000380562.2:n.*2753G>T
ENST00000426508.6:c.4315G>T	ENSP00000406012.2:p.Val1439Phe
ENST00000565298.5:n.4139G>T
NM_014714.3:c.4315G>T	NP_055529.2:p.Val1439Phe
XM_006720989.2:c.4315G>T	XP_006721052.1:p.Val1439Phe
XM_006720990.2:c.4315G>T	XP_006721053.1:p.Val1439Phe
XM_006720991.2:c.4315G>T	XP_006721054.1:p.Val1439Phe
XM_006720992.2:c.1948G>T	XP_006721055.1:p.Val650Phe
XM_011522766.1:c.4069G>T	XP_011521068.1:p.Val1357Phe
XM_011522767.1:c.3340G>T	XP_011521069.1:p.Val1114Phe
XM_006720990.3:c.4315G>T	XP_006721053.1:p.Val1439Phe
XM_006720991.3:c.4315G>T	XP_006721054.1:p.Val1439Phe
XM_006720992.3:c.1948G>T	XP_006721055.1:p.Val650Phe
XM_011522766.3:c.4069G>T	XP_011521068.1:p.Val1357Phe
XM_011522767.2:c.3340G>T	XP_011521069.1:p.Val1114Phe
XM_017023910.1:c.4315G>T	XP_016879399.1:p.Val1439Phe
XM_017023911.1:c.2500G>T	XP_016879400.1:p.Val834Phe
NM_014714.4:c.4315G>T MANE Select	NP_055529.2:p.Val1439Phe