Canonical Allele Identifier: CA1310558427

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636719_178636722delinsCAGG , CM000664.2:g.178636719_178636722delinsCAGG	GRCh38
NC_000002.11:g.179501446_179501449delinsCAGG , CM000664.1:g.179501446_179501449delinsCAGG	GRCh37
NC_000002.10:g.179209691_179209694delinsCAGG	NCBI36
NG_011618.3:g.199081_199084delinsCCTG , LRG_391:g.199081_199084delinsCCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33301_33304delinsCCTG	ENSP00000343764.6:p.Pro11101=
ENST00000342175.11:c.14386_14389delinsCCTG	ENSP00000340554.6:p.Pro4796=
ENST00000359218.10:c.14185_14188delinsCCTG	ENSP00000352154.5:p.Pro4729=
ENST00000342175.10:c.14386_14389delinsCCTG	ENSP00000340554.6:p.Pro4796=
ENST00000342992.10:c.33301_33304delinsCCTG	ENSP00000343764.6:p.Pro11101=
ENST00000359218.9:c.14185_14188delinsCCTG	ENSP00000352154.5:p.Pro4729=
ENST00000460472.6:c.13810_13813delinsCCTG	ENSP00000434586.1:p.Pro4604=
ENST00000589042.5:c.41005_41008delinsCCTG MANE Select	ENSP00000467141.1:p.Pro13669=
ENST00000591111.5:c.36082_36085delinsCCTG	ENSP00000465570.1:p.Pro12028=
ENST00000615779.4:c.36082_36085delinsCCTG	ENSP00000483597.1:p.Pro12028=
NM_001256850.1:c.36082_36085delinsCCTG	NP_001243779.1:p.Pro12028=
NM_001267550.2:c.41005_41008delinsCCTG MANE Select	NP_001254479.2:p.Pro13669=
NM_003319.4:c.13810_13813delinsCCTG	NP_003310.4:p.Pro4604=
NM_133378.4:c.33301_33304delinsCCTG	NP_596869.4:p.Pro11101=
NM_133432.3:c.14185_14188delinsCCTG	NP_597676.3:p.Pro4729=
NM_133437.4:c.14386_14389delinsCCTG	NP_597681.4:p.Pro4796=
XM_011511729.1:c.40102_40105delinsCCTG	XP_011510031.1:p.Pro13368=
XM_011511730.1:c.13996_13999delinsCCTG	XP_011510032.1:p.Pro4666=
XM_011511731.1:c.13855_13858delinsCCTG	XP_011510033.1:p.Pro4619=
XM_017004819.1:c.39898_39901delinsCCTG	XP_016860308.1:p.Pro13300=
XM_017004820.1:c.35296_35299delinsCCTG	XP_016860309.1:p.Pro11766=
XM_017004821.1:c.35293_35296delinsCCTG	XP_016860310.1:p.Pro11765=
XM_017004822.1:c.32335_32338delinsCCTG	XP_016860311.1:p.Pro10779=
XM_017004823.1:c.13951_13954delinsCCTG	XP_016860312.1:p.Pro4651=
XM_024453094.1:c.35446_35449delinsCCTG	XP_024308862.1:p.Pro11816=
XM_024453095.1:c.35443_35446delinsCCTG	XP_024308863.1:p.Pro11815=
XM_024453096.1:c.34876_34879delinsCCTG	XP_024308864.1:p.Pro11626=
XM_024453097.1:c.32218_32221delinsCCTG	XP_024308865.1:p.Pro10740=
XM_024453098.1:c.32137_32140delinsCCTG	XP_024308866.1:p.Pro10713=
XM_024453099.1:c.13900_13903delinsCCTG	XP_024308867.1:p.Pro4634=
XM_024453100.1:c.3754_3757delinsCCTG	XP_024308868.1:p.Pro1252=