Canonical Allele Identifier: CA349662618

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178639790T>C , CM000664.2:g.178639790T>C	GRCh38
NC_000002.11:g.179504517T>C , CM000664.1:g.179504517T>C	GRCh37
NC_000002.10:g.179212762T>C	NCBI36
NG_011618.3:g.196013A>G , LRG_391:g.196013A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.40787-2A>G MANE Select	NP_001254479.2:n.40787-2A>G
ENST00000589042.5:c.40787-2A>G MANE Select	ENSP00000467141.1:n.40787-2A>G
NM_001256850.1:c.35864-2A>G	NP_001243779.1:n.35864-2A>G
NM_003319.4:c.13592-2A>G	NP_003310.4:n.13592-2A>G
NM_133378.4:c.33083-2A>G	NP_596869.4:n.33083-2A>G
NM_133432.3:c.13967-2A>G	NP_597676.3:n.13967-2A>G
NM_133437.4:c.14168-2A>G	NP_597681.4:n.14168-2A>G
ENST00000342175.10:c.14168-2A>G	ENSP00000340554.6:n.14168-2A>G
ENST00000342175.11:c.14168-2A>G	ENSP00000340554.6:n.14168-2A>G
ENST00000342992.10:c.33083-2A>G	ENSP00000343764.6:n.33083-2A>G
ENST00000342992.11:c.33083-2A>G	ENSP00000343764.6:n.33083-2A>G
ENST00000359218.10:c.13967-2A>G	ENSP00000352154.5:n.13967-2A>G
ENST00000359218.9:c.13967-2A>G	ENSP00000352154.5:n.13967-2A>G
ENST00000414766.5:c.2750-2A>G	ENSP00000401501.1:n.2750-2A>G
ENST00000426232.5:c.750-2A>G
ENST00000460472.6:c.13592-2A>G	ENSP00000434586.1:n.13592-2A>G
ENST00000591111.5:c.35864-2A>G	ENSP00000465570.1:n.35864-2A>G
ENST00000615779.4:c.35864-2A>G	ENSP00000483597.1:n.35864-2A>G
XM_011511729.1:c.39884-2A>G	XP_011510031.1:n.39884-2A>G
XM_011511730.1:c.13778-2A>G	XP_011510032.1:n.13778-2A>G
XM_011511731.1:c.13637-2A>G	XP_011510033.1:n.13637-2A>G
XM_017004819.1:c.39680-2A>G	XP_016860308.1:n.39680-2A>G
XM_017004820.1:c.35078-2A>G	XP_016860309.1:n.35078-2A>G
XM_017004821.1:c.35075-2A>G	XP_016860310.1:n.35075-2A>G
XM_017004822.1:c.32168-2A>G	XP_016860311.1:n.32168-2A>G
XM_017004823.1:c.13733-2A>G	XP_016860312.1:n.13733-2A>G
XM_024453094.1:c.35228-2A>G	XP_024308862.1:n.35228-2A>G
XM_024453095.1:c.35225-2A>G	XP_024308863.1:n.35225-2A>G
XM_024453096.1:c.34658-2A>G	XP_024308864.1:n.34658-2A>G
XM_024453097.1:c.32000-2A>G	XP_024308865.1:n.32000-2A>G
XM_024453098.1:c.31919-2A>G	XP_024308866.1:n.31919-2A>G
XM_024453099.1:c.13733-2A>G	XP_024308867.1:n.13733-2A>G
XM_024453100.1:c.3536-2A>G	XP_024308868.1:n.3536-2A>G