Canonical Allele Identifier: CA2201723751

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520741A= , CM000678.2:g.1520741A=	GRCh38
NC_000016.9:g.1570742A= , CM000678.1:g.1570742A=	GRCh37
NC_000016.8:g.1510743A=	NCBI36
NG_032783.1:g.96368T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3521T= MANE Select	ENSP00000406012.2:p.Met1174=
ENST00000361339.9:c.1103T=	ENSP00000354895.5:p.Met368=
ENST00000397417.6:c.*1959T=	ENSP00000380562.2:n.*1959T=
ENST00000426508.6:c.3521T=	ENSP00000406012.2:p.Met1174=
ENST00000565298.5:n.3345T=
NM_014714.3:c.3521T=	NP_055529.2:p.Met1174=
XM_006720989.2:c.3521T=	XP_006721052.1:p.Met1174=
XM_006720990.2:c.3521T=	XP_006721053.1:p.Met1174=
XM_006720991.2:c.3521T=	XP_006721054.1:p.Met1174=
XM_006720992.2:c.1154T=	XP_006721055.1:p.Met385=
XM_011522766.1:c.3275T=	XP_011521068.1:p.Met1092=
XM_011522767.1:c.2546T=	XP_011521069.1:p.Met849=
XM_006720990.3:c.3521T=	XP_006721053.1:p.Met1174=
XM_006720991.3:c.3521T=	XP_006721054.1:p.Met1174=
XM_006720992.3:c.1154T=	XP_006721055.1:p.Met385=
XM_011522766.3:c.3275T=	XP_011521068.1:p.Met1092=
XM_011522767.2:c.2546T=	XP_011521069.1:p.Met849=
XM_017023910.1:c.3521T=	XP_016879399.1:p.Met1174=
XM_017023911.1:c.1706T=	XP_016879400.1:p.Met569=
NM_014714.4:c.3521T= MANE Select	NP_055529.2:p.Met1174=