Canonical Allele Identifier: CA223912

Gene: TTN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178713388_178713412dup , CM000664.2:g.178713388_178713412dup	GRCh38
NC_000002.11:g.179578115_179578139dup , CM000664.1:g.179578115_179578139dup	GRCh37
NC_000002.10:g.179286360_179286384dup	NCBI36
NG_011618.3:g.122397_122421dup , LRG_391:g.122397_122421dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.23030-34_23030-10dup	ENSP00000343764.6:n.23030-34_23030-10dup
ENST00000342175.11:c.13858+24676_13858+24700dup	ENSP00000340554.6:n.13858+24676_13858+24700dup
ENST00000359218.10:c.13657+24676_13657+24700dup	ENSP00000352154.5:n.13657+24676_13657+24700dup
ENST00000342175.10:c.13858+24676_13858+24700dup	ENSP00000340554.6:n.13858+24676_13858+24700dup
ENST00000342992.10:c.23030-34_23030-10dup	ENSP00000343764.6:n.23030-34_23030-10dup
ENST00000359218.9:c.13657+24676_13657+24700dup	ENSP00000352154.5:n.13657+24676_13657+24700dup
ENST00000460472.6:c.13282+24676_13282+24700dup	ENSP00000434586.1:n.13282+24676_13282+24700dup
ENST00000589042.5:c.26762-34_26762-10dup MANE Select	ENSP00000467141.1:n.26762-34_26762-10dup
ENST00000591111.5:c.25811-34_25811-10dup	ENSP00000465570.1:n.25811-34_25811-10dup
ENST00000615779.4:c.25811-34_25811-10dup	ENSP00000483597.1:n.25811-34_25811-10dup
NM_001256850.1:c.25811-34_25811-10dup	NP_001243779.1:n.25811-34_25811-10dup
NM_001267550.2:c.26762-34_26762-10dup MANE Select	NP_001254479.2:n.26762-34_26762-10dup
NM_003319.4:c.13282+24676_13282+24700dup	NP_003310.4:n.13282+24676_13282+24700dup
NM_133378.4:c.23030-34_23030-10dup	NP_596869.4:n.23030-34_23030-10dup
NM_133432.3:c.13657+24676_13657+24700dup	NP_597676.3:n.13657+24676_13657+24700dup
NM_133437.4:c.13858+24676_13858+24700dup	NP_597681.4:n.13858+24676_13858+24700dup
XM_011511729.1:c.25859-34_25859-10dup	XP_011510031.1:n.25859-34_25859-10dup
XM_011511730.1:c.13468+24676_13468+24700dup	XP_011510032.1:n.13468+24676_13468+24700dup
XM_011511731.1:c.13327+24676_13327+24700dup	XP_011510033.1:n.13327+24676_13327+24700dup
XM_017004819.1:c.25814-34_25814-10dup	XP_016860308.1:n.25814-34_25814-10dup
XM_017004820.1:c.23033-34_23033-10dup	XP_016860309.1:n.23033-34_23033-10dup
XM_017004821.1:c.23030-34_23030-10dup	XP_016860310.1:n.23030-34_23030-10dup
XM_017004822.1:c.25814-34_25814-10dup	XP_016860311.1:n.25814-34_25814-10dup
XM_017004823.1:c.13423+24676_13423+24700dup	XP_016860312.1:n.13423+24676_13423+24700dup
XM_024453094.1:c.25814-34_25814-10dup	XP_024308862.1:n.25814-34_25814-10dup
XM_024453095.1:c.25814-34_25814-10dup	XP_024308863.1:n.25814-34_25814-10dup
XM_024453096.1:c.25814-34_25814-10dup	XP_024308864.1:n.25814-34_25814-10dup
XM_024453097.1:c.25814-34_25814-10dup	XP_024308865.1:n.25814-34_25814-10dup
XM_024453098.1:c.25814-34_25814-10dup	XP_024308866.1:n.25814-34_25814-10dup
XM_024453099.1:c.13423+24676_13423+24700dup	XP_024308867.1:n.13423+24676_13423+24700dup