Canonical Allele Identifier: CA7812767

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510955C>T , CM000678.2:g.1510955C>T	GRCh38
NC_000016.9:g.1560956C>T , CM000678.1:g.1560956C>T	GRCh37
NC_000016.8:g.1500957C>T	NCBI36
NG_032783.1:g.106154G>A
NG_050910.1:g.22612C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.4378G>A MANE Select	NP_055529.2:p.Asp1460Asn
ENST00000426508.7:c.4378G>A MANE Select	ENSP00000406012.2:p.Asp1460Asn
NM_014714.3:c.4378G>A	NP_055529.2:p.Asp1460Asn
ENST00000361339.9:c.1960G>A	ENSP00000354895.5:p.Asp654Asn
ENST00000397417.6:c.*2816G>A	ENSP00000380562.2:n.*2816G>A
ENST00000426508.6:c.4378G>A	ENSP00000406012.2:p.Asp1460Asn
ENST00000565298.5:n.4202G>A
XM_006720989.2:c.4378G>A	XP_006721052.1:p.Asp1460Asn
XM_006720990.2:c.4378G>A	XP_006721053.1:p.Asp1460Asn
XM_006720990.3:c.4378G>A	XP_006721053.1:p.Asp1460Asn
XM_006720991.2:c.4378G>A	XP_006721054.1:p.Asp1460Asn
XM_006720991.3:c.4378G>A	XP_006721054.1:p.Asp1460Asn
XM_006720992.2:c.2011G>A	XP_006721055.1:p.Asp671Asn
XM_006720992.3:c.2011G>A	XP_006721055.1:p.Asp671Asn
XM_011522766.1:c.4132G>A	XP_011521068.1:p.Asp1378Asn
XM_011522766.3:c.4132G>A	XP_011521068.1:p.Asp1378Asn
XM_011522767.1:c.3403G>A	XP_011521069.1:p.Asp1135Asn
XM_011522767.2:c.3403G>A	XP_011521069.1:p.Asp1135Asn
XM_017023910.1:c.4378G>A	XP_016879399.1:p.Asp1460Asn
XM_017023911.1:c.2563G>A	XP_016879400.1:p.Asp855Asn