Canonical Allele Identifier: CA1310530786

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569883T= , CM000664.2:g.178569883T=	GRCh38
NC_000002.11:g.179434610T= , CM000664.1:g.179434610T=	GRCh37
NC_000002.10:g.179142856T=	NCBI36
NG_011618.3:g.265920A= , LRG_391:g.265920A=
NG_051363.1:g.52057T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.68545A= (TTN)	ENSP00000343764.6:p.Ile22849=
ENST00000342175.11:c.49630A= (TTN)	ENSP00000340554.6:p.Ile16544=
ENST00000359218.10:c.49429A= (TTN)	ENSP00000352154.5:p.Ile16477=
ENST00000342175.10:c.49630A= (TTN)	ENSP00000340554.6:p.Ile16544=
ENST00000342992.10:c.68545A= (TTN)	ENSP00000343764.6:p.Ile22849=
ENST00000359218.9:c.49429A= (TTN)	ENSP00000352154.5:p.Ile16477=
ENST00000460472.6:c.49054A= (TTN)	ENSP00000434586.1:p.Ile16352=
ENST00000589042.5:c.76249A= (TTN) MANE Select	ENSP00000467141.1:p.Ile25417=
ENST00000591111.5:c.71326A= (TTN)	ENSP00000465570.1:p.Ile23776=
ENST00000615779.4:c.71326A= (TTN)	ENSP00000483597.1:p.Ile23776=
NM_001256850.1:c.71326A= (TTN)	NP_001243779.1:p.Ile23776=
NM_001267550.2:c.76249A= (TTN) MANE Select	NP_001254479.2:p.Ile25417=
NM_003319.4:c.49054A= (TTN)	NP_003310.4:p.Ile16352=
NM_133378.4:c.68545A= (TTN)	NP_596869.4:p.Ile22849=
NM_133432.3:c.49429A= (TTN)	NP_597676.3:p.Ile16477=
NM_133437.4:c.49630A= (TTN)	NP_597681.4:p.Ile16544=
NR_038271.1:n.447-1417T= (TTN-AS1)
NR_038272.1:n.2044-12689T= (TTN-AS1)
XM_011511729.1:c.75346A= (TTN)	XP_011510031.1:p.Ile25116=
XM_011511730.1:c.49240A= (TTN)	XP_011510032.1:p.Ile16414=
XM_011511731.1:c.49099A= (TTN)	XP_011510033.1:p.Ile16367=
XM_017004819.1:c.75142A= (TTN)	XP_016860308.1:p.Ile25048=
XM_017004820.1:c.70540A= (TTN)	XP_016860309.1:p.Ile23514=
XM_017004821.1:c.70537A= (TTN)	XP_016860310.1:p.Ile23513=
XM_017004822.1:c.67579A= (TTN)	XP_016860311.1:p.Ile22527=
XM_017004823.1:c.49195A= (TTN)	XP_016860312.1:p.Ile16399=
XM_024453094.1:c.70690A= (TTN)	XP_024308862.1:p.Ile23564=
XM_024453095.1:c.70687A= (TTN)	XP_024308863.1:p.Ile23563=
XM_024453096.1:c.70120A= (TTN)	XP_024308864.1:p.Ile23374=
XM_024453097.1:c.67462A= (TTN)	XP_024308865.1:p.Ile22488=
XM_024453098.1:c.67381A= (TTN)	XP_024308866.1:p.Ile22461=
XM_024453099.1:c.49144A= (TTN)	XP_024308867.1:p.Ile16382=
XM_024453100.1:c.38998A= (TTN)	XP_024308868.1:p.Ile13000=