Canonical Allele Identifier: CA394205994

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1616214C>A (hg19) ; chr16:g.1566213C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1566213C>A , CM000678.2:g.1566213C>A	GRCh38
NC_000016.9:g.1616214C>A , CM000678.1:g.1616214C>A	GRCh37
NC_000016.8:g.1556215C>A	NCBI36
NG_032783.1:g.50896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.1849G>T MANE Select	ENSP00000406012.2:p.Gly617Ter
ENST00000397417.6:c.*401G>T	ENSP00000380562.2:n.*401G>T
ENST00000426508.6:c.1849G>T	ENSP00000406012.2:p.Gly617Ter
ENST00000439987.6:n.1910G>T
ENST00000565298.5:n.537G>T
NM_014714.3:c.1849G>T	NP_055529.2:p.Gly617Ter
XM_005255725.3:c.1849G>T	XP_005255782.1:p.Gly617Ter
XM_005255726.2:c.1849G>T	XP_005255783.1:p.Gly617Ter
XM_006720989.2:c.1849G>T	XP_006721052.1:p.Gly617Ter
XM_006720990.2:c.1849G>T	XP_006721053.1:p.Gly617Ter
XM_006720991.2:c.1849G>T	XP_006721054.1:p.Gly617Ter
XM_011522766.1:c.1603G>T	XP_011521068.1:p.Gly535Ter
XM_011522767.1:c.874G>T	XP_011521069.1:p.Gly292Ter
XM_011522768.1:c.1849G>T	XP_011521070.1:p.Gly617Ter
XM_011522769.1:c.1849G>T	XP_011521071.1:p.Gly617Ter
XM_011522771.1:c.1849G>T	XP_011521073.1:p.Gly617Ter
XM_011522772.1:c.1849G>T	XP_011521074.1:p.Gly617Ter
XM_005255725.5:c.1849G>T	XP_005255782.1:p.Gly617Ter
XM_005255726.4:c.1849G>T	XP_005255783.1:p.Gly617Ter
XM_006720990.3:c.1849G>T	XP_006721053.1:p.Gly617Ter
XM_006720991.3:c.1849G>T	XP_006721054.1:p.Gly617Ter
XM_011522766.3:c.1603G>T	XP_011521068.1:p.Gly535Ter
XM_011522767.2:c.874G>T	XP_011521069.1:p.Gly292Ter
XM_011522769.3:c.1849G>T	XP_011521071.1:p.Gly617Ter
XM_011522771.3:c.1849G>T	XP_011521073.1:p.Gly617Ter
XM_011522772.3:c.1849G>T	XP_011521074.1:p.Gly617Ter
XM_017023910.1:c.1849G>T	XP_016879399.1:p.Gly617Ter
XM_017023911.1:c.34G>T	XP_016879400.1:p.Gly12Ter
NM_014714.4:c.1849G>T MANE Select	NP_055529.2:p.Gly617Ter