Canonical Allele Identifier: CA1310511575

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530144A= , CM000664.2:g.178530144A=	GRCh38
NC_000002.11:g.179394871A= , CM000664.1:g.179394871A=	GRCh37
NC_000002.10:g.179103117A=	NCBI36
NG_011618.3:g.305659T= , LRG_391:g.305659T=
NG_051363.1:g.12318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98671-28T= (TTN)	ENSP00000343764.6:n.98671-28T=
ENST00000342175.11:c.79756-28T= (TTN)	ENSP00000340554.6:n.79756-28T=
ENST00000359218.10:c.79555-28T= (TTN)	ENSP00000352154.5:n.79555-28T=
ENST00000342175.10:c.79756-28T= (TTN)	ENSP00000340554.6:n.79756-28T=
ENST00000342992.10:c.98671-28T= (TTN)	ENSP00000343764.6:n.98671-28T=
ENST00000359218.9:c.79555-28T= (TTN)	ENSP00000352154.5:n.79555-28T=
ENST00000460472.6:c.79180-28T= (TTN)	ENSP00000434586.1:n.79180-28T=
ENST00000589042.5:c.106375-28T= (TTN) MANE Select	ENSP00000467141.1:n.106375-28T=
ENST00000591111.5:c.101452-28T= (TTN)	ENSP00000465570.1:n.101452-28T=
ENST00000615779.4:c.101452-28T= (TTN)	ENSP00000483597.1:n.101452-28T=
NM_001256850.1:c.101452-28T= (TTN)	NP_001243779.1:n.101452-28T=
NM_001267550.2:c.106375-28T= (TTN) MANE Select	NP_001254479.2:n.106375-28T=
NM_003319.4:c.79180-28T= (TTN)	NP_003310.4:n.79180-28T=
NM_133378.4:c.98671-28T= (TTN)	NP_596869.4:n.98671-28T=
NM_133432.3:c.79555-28T= (TTN)	NP_597676.3:n.79555-28T=
NM_133437.4:c.79756-28T= (TTN)	NP_597681.4:n.79756-28T=
NR_038271.1:n.446+6508A= (TTN-AS1)
NR_038272.1:n.220-5588A= (TTN-AS1)
XM_011511729.1:c.105472-28T= (TTN)	XP_011510031.1:n.105472-28T=
XM_011511730.1:c.79366-28T= (TTN)	XP_011510032.1:n.79366-28T=
XM_011511731.1:c.79225-28T= (TTN)	XP_011510033.1:n.79225-28T=
XM_017004819.1:c.105268-28T= (TTN)	XP_016860308.1:n.105268-28T=
XM_017004820.1:c.100666-28T= (TTN)	XP_016860309.1:n.100666-28T=
XM_017004821.1:c.100663-28T= (TTN)	XP_016860310.1:n.100663-28T=
XM_017004822.1:c.97705-28T= (TTN)	XP_016860311.1:n.97705-28T=
XM_017004823.1:c.79321-28T= (TTN)	XP_016860312.1:n.79321-28T=
XM_024453094.1:c.100816-28T= (TTN)	XP_024308862.1:n.100816-28T=
XM_024453095.1:c.100813-28T= (TTN)	XP_024308863.1:n.100813-28T=
XM_024453096.1:c.100246-28T= (TTN)	XP_024308864.1:n.100246-28T=
XM_024453097.1:c.97588-28T= (TTN)	XP_024308865.1:n.97588-28T=
XM_024453098.1:c.97507-28T= (TTN)	XP_024308866.1:n.97507-28T=
XM_024453099.1:c.79270-28T= (TTN)	XP_024308867.1:n.79270-28T=
XM_024453100.1:c.69124-28T= (TTN)	XP_024308868.1:n.69124-28T=