Canonical Allele Identifier: CA492928723

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1639738C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1589737C>A , CM000678.2:g.1589737C>A	GRCh38
NC_000016.9:g.1639738C>A , CM000678.1:g.1639738C>A	GRCh37
NC_000016.8:g.1579739C>A	NCBI36
NG_032783.1:g.27372G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.678G>T MANE Select	ENSP00000406012.2:p.Val226=
ENST00000397417.6:c.329-5317G>T	ENSP00000380562.2:n.329-5317G>T
ENST00000426508.6:c.678G>T	ENSP00000406012.2:p.Val226=
ENST00000439987.6:n.739G>T
NM_014714.3:c.678G>T	NP_055529.2:p.Val226=
XM_005255725.3:c.678G>T	XP_005255782.1:p.Val226=
XM_005255726.2:c.678G>T	XP_005255783.1:p.Val226=
XM_006720989.2:c.678G>T	XP_006721052.1:p.Val226=
XM_006720990.2:c.678G>T	XP_006721053.1:p.Val226=
XM_006720991.2:c.678G>T	XP_006721054.1:p.Val226=
XM_011522766.1:c.678G>T	XP_011521068.1:p.Val226=
XM_011522768.1:c.678G>T	XP_011521070.1:p.Val226=
XM_011522769.1:c.678G>T	XP_011521071.1:p.Val226=
XM_011522771.1:c.678G>T	XP_011521073.1:p.Val226=
XM_011522772.1:c.678G>T	XP_011521074.1:p.Val226=
NR_135176.1:n.59+9152C>A
XM_005255725.5:c.678G>T	XP_005255782.1:p.Val226=
XM_005255726.4:c.678G>T	XP_005255783.1:p.Val226=
XM_006720990.3:c.678G>T	XP_006721053.1:p.Val226=
XM_006720991.3:c.678G>T	XP_006721054.1:p.Val226=
XM_011522766.3:c.678G>T	XP_011521068.1:p.Val226=
XM_011522769.3:c.678G>T	XP_011521071.1:p.Val226=
XM_011522771.3:c.678G>T	XP_011521073.1:p.Val226=
XM_011522772.3:c.678G>T	XP_011521074.1:p.Val226=
XM_017023910.1:c.678G>T	XP_016879399.1:p.Val226=
XM_017023911.1:c.-1020G>T	XP_016879400.1:n.-1020G>T
NM_014714.4:c.678G>T MANE Select	NP_055529.2:p.Val226=