Canonical Allele Identifier: CA493031298

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1569932C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1519931C>G , CM000678.2:g.1519931C>G	GRCh38
NC_000016.9:g.1569932C>G , CM000678.1:g.1569932C>G	GRCh37
NC_000016.8:g.1509933C>G	NCBI36
NG_032783.1:g.97178G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3990G>C MANE Select	ENSP00000406012.2:p.Ala1330=
ENST00000361339.9:c.1572G>C	ENSP00000354895.5:p.Ala524=
ENST00000397417.6:c.*2428G>C	ENSP00000380562.2:n.*2428G>C
ENST00000426508.6:c.3990G>C	ENSP00000406012.2:p.Ala1330=
ENST00000565298.5:n.3814G>C
ENST00000568837.1:c.108G>C	ENSP00000458439.1:p.Ala36=
NM_014714.3:c.3990G>C	NP_055529.2:p.Ala1330=
XM_006720989.2:c.3990G>C	XP_006721052.1:p.Ala1330=
XM_006720990.2:c.3990G>C	XP_006721053.1:p.Ala1330=
XM_006720991.2:c.3990G>C	XP_006721054.1:p.Ala1330=
XM_006720992.2:c.1623G>C	XP_006721055.1:p.Ala541=
XM_011522766.1:c.3744G>C	XP_011521068.1:p.Ala1248=
XM_011522767.1:c.3015G>C	XP_011521069.1:p.Ala1005=
XM_006720990.3:c.3990G>C	XP_006721053.1:p.Ala1330=
XM_006720991.3:c.3990G>C	XP_006721054.1:p.Ala1330=
XM_006720992.3:c.1623G>C	XP_006721055.1:p.Ala541=
XM_011522766.3:c.3744G>C	XP_011521068.1:p.Ala1248=
XM_011522767.2:c.3015G>C	XP_011521069.1:p.Ala1005=
XM_017023910.1:c.3990G>C	XP_016879399.1:p.Ala1330=
XM_017023911.1:c.2175G>C	XP_016879400.1:p.Ala725=
NM_014714.4:c.3990G>C MANE Select	NP_055529.2:p.Ala1330=