Canonical Allele Identifier: CA7813557
Community Standard Title: NM_014714.4(IFT140):c.2598C>G (p.Tyr866Ter)
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1526057G>C , CM000678.2:g.1526057G>C GRCh38
NC_000016.9:g.1576058G>C , CM000678.1:g.1576058G>C GRCh37
NC_000016.8:g.1516059G>C NCBI36
NG_032783.1:g.91052C>G

Transcript Alleles

HGVS Amino-acid Change
NM_014714.4:c.2598C>G MANE Select NP_055529.2:p.Tyr866Ter
ENST00000426508.7:c.2598C>G MANE Select ENSP00000406012.2:p.Tyr866Ter
NM_014714.3:c.2598C>G NP_055529.2:p.Tyr866Ter
ENST00000361339.9:c.180C>G ENSP00000354895.5:p.Tyr60Ter
ENST00000397417.6:c.*1036C>G ENSP00000380562.2:n.*1036C>G
ENST00000426508.6:c.2598C>G ENSP00000406012.2:p.Tyr866Ter
ENST00000565298.5:n.1827C>G
ENST00000566818.1:n.313C>G
XM_006720989.2:c.2598C>G XP_006721052.1:p.Tyr866Ter
XM_006720990.2:c.2598C>G XP_006721053.1:p.Tyr866Ter
XM_006720990.3:c.2598C>G XP_006721053.1:p.Tyr866Ter
XM_006720991.2:c.2598C>G XP_006721054.1:p.Tyr866Ter
XM_006720991.3:c.2598C>G XP_006721054.1:p.Tyr866Ter
XM_006720992.2:c.231C>G XP_006721055.1:p.Tyr77Ter
XM_006720992.3:c.231C>G XP_006721055.1:p.Tyr77Ter
XM_011522766.1:c.2352C>G XP_011521068.1:p.Tyr784Ter
XM_011522766.3:c.2352C>G XP_011521068.1:p.Tyr784Ter
XM_011522767.1:c.1623C>G XP_011521069.1:p.Tyr541Ter
XM_011522767.2:c.1623C>G XP_011521069.1:p.Tyr541Ter
XM_017023910.1:c.2598C>G XP_016879399.1:p.Tyr866Ter
XM_017023911.1:c.783C>G XP_016879400.1:p.Tyr261Ter