Canonical Allele Identifier: CA2631005892

Gene: IFT140

Linked Data

• gnomAD v4: 16-1510573-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510573A>G , CM000678.2:g.1510573A>G	GRCh38
NC_000016.9:g.1560574A>G , CM000678.1:g.1560574A>G	GRCh37
NC_000016.8:g.1500575A>G	NCBI36
NG_032783.1:g.106536T>C
NG_050910.1:g.22230A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.*371T>C MANE Select	ENSP00000406012.2:n.*371T>C
ENST00000361339.9:c.*371T>C	ENSP00000354895.5:n.*371T>C
ENST00000397417.6:c.*3198T>C	ENSP00000380562.2:n.*3198T>C
ENST00000426508.6:c.*371T>C	ENSP00000406012.2:n.*371T>C
ENST00000565298.5:n.4584T>C
NM_014714.3:c.*371T>C	NP_055529.2:n.*371T>C
XM_006720989.2:c.*371T>C	XP_006721052.1:n.*371T>C
XM_006720990.2:c.*371T>C	XP_006721053.1:n.*371T>C
XM_006720991.2:c.*371T>C	XP_006721054.1:n.*371T>C
XM_006720992.2:c.*371T>C	XP_006721055.1:n.*371T>C
XM_011522766.1:c.*371T>C	XP_011521068.1:n.*371T>C
XM_011522767.1:c.*371T>C	XP_011521069.1:n.*371T>C
XM_006720990.3:c.*371T>C	XP_006721053.1:n.*371T>C
XM_006720991.3:c.*371T>C	XP_006721054.1:n.*371T>C
XM_006720992.3:c.*371T>C	XP_006721055.1:n.*371T>C
XM_011522766.3:c.*371T>C	XP_011521068.1:n.*371T>C
XM_011522767.2:c.*371T>C	XP_011521069.1:n.*371T>C
XM_017023910.1:c.*371T>C	XP_016879399.1:n.*371T>C
XM_017023911.1:c.*371T>C	XP_016879400.1:n.*371T>C
NM_014714.4:c.*371T>C MANE Select	NP_055529.2:n.*371T>C