Canonical Allele Identifier: CA5096942

Gene: TLE1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.81584467T>C , CM000671.2:g.81584467T>C	GRCh38
NC_000009.11:g.84199382T>C , CM000671.1:g.84199382T>C	GRCh37
NC_000009.10:g.83389202T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376499.8:c.2186A>G MANE Select	ENSP00000365682.3:p.Tyr729Cys
ENST00000376472.5:c.2183A>G	ENSP00000365655.2:p.Tyr728Cys
ENST00000376499.7:c.2186A>G	ENSP00000365682.3:p.Tyr729Cys
NM_001303103.1:c.2216A>G	NP_001290032.1:p.Tyr739Cys
NM_001303104.1:c.2141A>G	NP_001290033.1:p.Tyr714Cys
NM_005077.4:c.2186A>G	NP_005068.2:p.Tyr729Cys
XM_005252151.1:c.2318A>G	XP_005252208.1:p.Tyr773Cys
XM_005252152.1:c.2315A>G	XP_005252209.1:p.Tyr772Cys
XM_005252153.1:c.2288A>G	XP_005252210.1:p.Tyr763Cys
XM_005252154.1:c.2285A>G	XP_005252211.1:p.Tyr762Cys
XM_005252156.1:c.2213A>G	XP_005252213.1:p.Tyr738Cys
XM_005252162.1:c.2066A>G	XP_005252219.1:p.Tyr689Cys
XM_005252163.1:c.1964A>G	XP_005252220.1:p.Tyr655Cys
XM_006717258.1:c.2315A>G	XP_006717321.1:p.Tyr772Cys
XM_006717259.2:c.2150A>G	XP_006717322.1:p.Tyr717Cys
XM_006717260.1:c.2096A>G	XP_006717323.1:p.Tyr699Cys
XM_006717261.2:c.1973A>G	XP_006717324.1:p.Tyr658Cys
XM_006717262.1:c.2183A>G	XP_006717325.1:p.Tyr728Cys
XM_006717263.1:c.2180A>G	XP_006717326.1:p.Tyr727Cys
XM_011518951.1:c.2183A>G	XP_011517253.1:p.Tyr728Cys
XM_005252156.3:c.2213A>G	XP_005252213.1:p.Tyr738Cys
XM_005252163.2:c.1964A>G	XP_005252220.1:p.Tyr655Cys
XM_006717259.4:c.2150A>G	XP_006717322.1:p.Tyr717Cys
XM_011518951.2:c.2183A>G	XP_011517253.1:p.Tyr728Cys
XM_017015064.1:c.2213A>G	XP_016870553.1:p.Tyr738Cys
XM_017015065.1:c.2210A>G	XP_016870554.1:p.Tyr737Cys
XM_017015066.1:c.2048A>G	XP_016870555.1:p.Tyr683Cys
NM_005077.5:c.2186A>G MANE Select	NP_005068.2:p.Tyr729Cys
NM_001303103.2:c.2216A>G	NP_001290032.1:p.Tyr739Cys
NM_001303104.2:c.2141A>G	NP_001290033.1:p.Tyr714Cys