Canonical Allele Identifier: CA493032025

Gene: IFT140

Linked Data

• ClinVar Variation Id: 1154317
• ClinVar RCV Id: RCV001496267
• dbSNP Id: rs771939015
• gnomAD v2: 16-1573669-G-A
• gnomAD v3: 16-1523668-G-A
• gnomAD v4: 16-1523668-G-A
• MyVariant Identifiers: chr16:g.1573669G>A (hg19) ; chr16:g.1523668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523668G>A , CM000678.2:g.1523668G>A	GRCh38
NC_000016.9:g.1573669G>A , CM000678.1:g.1573669G>A	GRCh37
NC_000016.8:g.1513670G>A	NCBI36
NG_032783.1:g.93441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3303C>T MANE Select	ENSP00000406012.2:p.Ala1101=
ENST00000361339.9:c.885C>T	ENSP00000354895.5:p.Ala295=
ENST00000397417.6:c.*1741C>T	ENSP00000380562.2:n.*1741C>T
ENST00000426508.6:c.3303C>T	ENSP00000406012.2:p.Ala1101=
ENST00000565298.5:n.3127C>T
NM_014714.3:c.3303C>T	NP_055529.2:p.Ala1101=
XM_006720989.2:c.3303C>T	XP_006721052.1:p.Ala1101=
XM_006720990.2:c.3303C>T	XP_006721053.1:p.Ala1101=
XM_006720991.2:c.3303C>T	XP_006721054.1:p.Ala1101=
XM_006720992.2:c.936C>T	XP_006721055.1:p.Ala312=
XM_011522766.1:c.3057C>T	XP_011521068.1:p.Ala1019=
XM_011522767.1:c.2328C>T	XP_011521069.1:p.Ala776=
XM_006720990.3:c.3303C>T	XP_006721053.1:p.Ala1101=
XM_006720991.3:c.3303C>T	XP_006721054.1:p.Ala1101=
XM_006720992.3:c.936C>T	XP_006721055.1:p.Ala312=
XM_011522766.3:c.3057C>T	XP_011521068.1:p.Ala1019=
XM_011522767.2:c.2328C>T	XP_011521069.1:p.Ala776=
XM_017023910.1:c.3303C>T	XP_016879399.1:p.Ala1101=
XM_017023911.1:c.1488C>T	XP_016879400.1:p.Ala496=
NM_014714.4:c.3303C>T MANE Select	NP_055529.2:p.Ala1101=