Canonical Allele Identifier: CA351713922

Gene: TTLL3 ARPC4-TTLL3

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9826996G>C , CM000665.2:g.9826996G>C	GRCh38
NC_000003.11:g.9868680G>C , CM000665.1:g.9868680G>C	GRCh37
NC_000003.10:g.9843680G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703870.1:c.1004-1G>C (TTLL3)	ENSP00000515513.1:n.1004-1G>C
ENST00000426895.10:c.875-1G>C (TTLL3)	ENSP00000392549.5:n.875-1G>C
ENST00000685419.1:c.1004-1G>C (TTLL3) MANE Select	ENSP00000510679.1:n.1004-1G>C
ENST00000426895.9:c.1304-1G>C (TTLL3)	ENSP00000392549.4:n.1304-1G>C
ENST00000310252.11:c.741-1G>C (TTLL3)
ENST00000383827.5:c.239-1G>C (TTLL3)	ENSP00000373338.1:n.239-1G>C
ENST00000397256.5:c.1058-1G>C (ARPC4-TTLL3)	ENSP00000380427.1:n.1058-1G>C
ENST00000426895.8:c.1304-1G>C (TTLL3)	ENSP00000392549.4:n.1304-1G>C
ENST00000427220.5:c.*659-1G>C (TTLL3)	ENSP00000395912.1:n.*659-1G>C
ENST00000430390.5:c.457-1G>C (TTLL3)
ENST00000430793.1:c.239-1G>C (TTLL3)	ENSP00000403874.1:n.239-1G>C
ENST00000431204.5:c.316-1G>C (TTLL3)	ENSP00000398996.1:n.316-1G>C
ENST00000438141.5:c.239-1G>C (TTLL3)	ENSP00000409246.1:n.239-1G>C
ENST00000443148.5:c.689-1G>C (TTLL3)	ENSP00000398097.1:n.689-1G>C
ENST00000455274.5:c.239-1G>C (TTLL3)	ENSP00000409632.1:n.239-1G>C
ENST00000466245.1:n.89-1G>C (TTLL3)
ENST00000473661.5:c.239-1G>C (TTLL3)	ENSP00000430051.1:n.239-1G>C
ENST00000482269.1:n.544-1G>C (TTLL3)
ENST00000483051.5:n.1720-1G>C (TTLL3)
ENST00000492440.1:n.384-1G>C (TTLL3)
ENST00000496526.5:n.3419-1G>C (TTLL3)
NM_001025930.3:c.1304-1G>C (TTLL3)	NP_001021100.3:n.1304-1G>C
NM_001198793.1:c.1058-1G>C (ARPC4-TTLL3)	NP_001185722.1:n.1058-1G>C
NR_037162.1:n.1973-1G>C (TTLL3)
NM_001025930.4:c.1304-1G>C (TTLL3)	NP_001021100.3:n.1304-1G>C
NM_001366051.1:c.875-1G>C (TTLL3)	NP_001352980.1:n.875-1G>C
NM_001025930.5:c.1304-1G>C (TTLL3)	NP_001021100.3:n.1304-1G>C
NM_001366051.2:c.875-1G>C (TTLL3)	NP_001352980.1:n.875-1G>C
NR_037162.2:n.1671-1G>C (TTLL3)
NM_001387446.1:c.1004-1G>C (TTLL3) MANE Select	NP_001374375.1:n.1004-1G>C
NM_001387447.1:c.1004-1G>C (TTLL3)	NP_001374376.1:n.1004-1G>C
NM_001387448.1:c.875-1G>C (TTLL3)	NP_001374377.1:n.875-1G>C
NM_001387449.1:c.875-1G>C (TTLL3)	NP_001374378.1:n.875-1G>C
NM_001387450.1:c.1049-1G>C (TTLL3)	NP_001374379.1:n.1049-1G>C
NM_001387451.1:c.905-1G>C (TTLL3)	NP_001374380.1:n.905-1G>C
NM_001387452.1:c.776-1G>C (TTLL3)	NP_001374381.1:n.776-1G>C
NM_001387453.1:c.776-1G>C (TTLL3)	NP_001374382.1:n.776-1G>C
NM_001387454.1:c.1004-1G>C (TTLL3)	NP_001374383.1:n.1004-1G>C
NM_001387455.1:c.1004-1G>C (TTLL3)	NP_001374384.1:n.1004-1G>C
NM_001387456.1:c.1004-1G>C (TTLL3)	NP_001374385.1:n.1004-1G>C
NM_001387457.1:c.1004-1G>C (TTLL3)	NP_001374386.1:n.1004-1G>C
NM_001387458.1:c.776-1G>C (TTLL3)	NP_001374387.1:n.776-1G>C
NM_001387459.1:c.905-1G>C (TTLL3)	NP_001374388.1:n.905-1G>C
NM_001387460.1:c.905-1G>C (TTLL3)	NP_001374389.1:n.905-1G>C
NM_001387461.1:c.875-1G>C (TTLL3)	NP_001374390.1:n.875-1G>C
NM_001387462.1:c.872-1G>C (TTLL3)	NP_001374391.1:n.872-1G>C
NM_001387463.1:c.776-1G>C (TTLL3)	NP_001374392.1:n.776-1G>C
NM_001387464.1:c.905-1G>C (TTLL3)	NP_001374393.1:n.905-1G>C
NM_001387465.1:c.905-1G>C (TTLL3)	NP_001374394.1:n.905-1G>C
NM_001387466.1:c.512-1G>C (TTLL3)	NP_001374395.1:n.512-1G>C
NM_001387467.1:c.239-1G>C (TTLL3)	NP_001374396.1:n.239-1G>C
NR_170661.1:n.1013-1G>C (TTLL3)
NR_170662.1:n.686-1G>C (TTLL3)
NR_170663.1:n.639-1G>C (TTLL3)
NR_170664.1:n.801-1G>C (TTLL3)
NR_170665.1:n.835-1G>C (TTLL3)