Canonical Allele Identifier: CA7814367

Gene: IFT140

Linked Data

• ClinVar Variation Id: 961914
• ClinVar RCV Id: RCV001235678
• dbSNP Id: rs538562131
• ExAC: 16:1634250 C / T
• gnomAD v2: 16-1634250-C-T
• gnomAD v3: 16-1584249-C-T
• gnomAD v4: 16-1584249-C-T
• MyVariant Identifiers: chr16:g.1634250C>T (hg19) ; chr16:g.1584249C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1584249C>T , CM000678.2:g.1584249C>T	GRCh38
NC_000016.9:g.1634250C>T , CM000678.1:g.1634250C>T	GRCh37
NC_000016.8:g.1574251C>T	NCBI36
NG_032783.1:g.32860G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.1327G>A MANE Select	ENSP00000406012.2:p.Asp443Asn
ENST00000397417.6:c.500G>A	ENSP00000380562.2:p.Arg167Gln
ENST00000426508.6:c.1327G>A	ENSP00000406012.2:p.Asp443Asn
ENST00000439987.6:n.1388G>A
ENST00000565298.5:n.15G>A
NM_014714.3:c.1327G>A	NP_055529.2:p.Asp443Asn
XM_005255725.3:c.1327G>A	XP_005255782.1:p.Asp443Asn
XM_005255726.2:c.1327G>A	XP_005255783.1:p.Asp443Asn
XM_006720989.2:c.1327G>A	XP_006721052.1:p.Asp443Asn
XM_006720990.2:c.1327G>A	XP_006721053.1:p.Asp443Asn
XM_006720991.2:c.1327G>A	XP_006721054.1:p.Asp443Asn
XM_011522766.1:c.1327G>A	XP_011521068.1:p.Asp443Asn
XM_011522767.1:c.352G>A	XP_011521069.1:p.Asp118Asn
XM_011522768.1:c.1327G>A	XP_011521070.1:p.Asp443Asn
XM_011522769.1:c.1327G>A	XP_011521071.1:p.Asp443Asn
XM_011522771.1:c.1327G>A	XP_011521073.1:p.Asp443Asn
XM_011522772.1:c.1327G>A	XP_011521074.1:p.Asp443Asn
NR_135176.1:n.59+3664C>T
XM_005255725.5:c.1327G>A	XP_005255782.1:p.Asp443Asn
XM_005255726.4:c.1327G>A	XP_005255783.1:p.Asp443Asn
XM_006720990.3:c.1327G>A	XP_006721053.1:p.Asp443Asn
XM_006720991.3:c.1327G>A	XP_006721054.1:p.Asp443Asn
XM_011522766.3:c.1327G>A	XP_011521068.1:p.Asp443Asn
XM_011522767.2:c.352G>A	XP_011521069.1:p.Asp118Asn
XM_011522769.3:c.1327G>A	XP_011521071.1:p.Asp443Asn
XM_011522771.3:c.1327G>A	XP_011521073.1:p.Asp443Asn
XM_011522772.3:c.1327G>A	XP_011521074.1:p.Asp443Asn
XM_017023910.1:c.1327G>A	XP_016879399.1:p.Asp443Asn
XM_017023911.1:c.-371G>A	XP_016879400.1:n.-371G>A
NM_014714.4:c.1327G>A MANE Select	NP_055529.2:p.Asp443Asn