Canonical Allele Identifier: CA430241429

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408064G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543337G>T , CM000664.2:g.178543337G>T	GRCh38
NC_000002.11:g.179408064G>T , CM000664.1:g.179408064G>T	GRCh37
NC_000002.10:g.179116310G>T	NCBI36
NG_011618.3:g.292466C>A , LRG_391:g.292466C>A
NG_051363.1:g.25511G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88932C>A (TTN)	ENSP00000343764.6:p.Val29644=
ENST00000342175.11:c.70017C>A (TTN)	ENSP00000340554.6:p.Val23339=
ENST00000359218.10:c.69816C>A (TTN)	ENSP00000352154.5:p.Val23272=
ENST00000342175.10:c.70017C>A (TTN)	ENSP00000340554.6:p.Val23339=
ENST00000342992.10:c.88932C>A (TTN)	ENSP00000343764.6:p.Val29644=
ENST00000359218.9:c.69816C>A (TTN)	ENSP00000352154.5:p.Val23272=
ENST00000460472.6:c.69441C>A (TTN)	ENSP00000434586.1:p.Val23147=
ENST00000589042.5:c.96636C>A (TTN) MANE Select	ENSP00000467141.1:p.Val32212=
ENST00000591111.5:c.91713C>A (TTN)	ENSP00000465570.1:p.Val30571=
ENST00000615779.4:c.91713C>A (TTN)	ENSP00000483597.1:p.Val30571=
NM_001256850.1:c.91713C>A (TTN)	NP_001243779.1:p.Val30571=
NM_001267550.2:c.96636C>A (TTN) MANE Select	NP_001254479.2:p.Val32212=
NM_003319.4:c.69441C>A (TTN)	NP_003310.4:p.Val23147=
NM_133378.4:c.88932C>A (TTN)	NP_596869.4:p.Val29644=
NM_133432.3:c.69816C>A (TTN)	NP_597676.3:p.Val23272=
NM_133437.4:c.70017C>A (TTN)	NP_597681.4:p.Val23339=
NR_038271.1:n.446+19701G>T (TTN-AS1)
NR_038272.1:n.2043+976G>T (TTN-AS1)
XM_011511729.1:c.95733C>A (TTN)	XP_011510031.1:p.Val31911=
XM_011511730.1:c.69627C>A (TTN)	XP_011510032.1:p.Val23209=
XM_011511731.1:c.69486C>A (TTN)	XP_011510033.1:p.Val23162=
XM_017004819.1:c.95529C>A (TTN)	XP_016860308.1:p.Val31843=
XM_017004820.1:c.90927C>A (TTN)	XP_016860309.1:p.Val30309=
XM_017004821.1:c.90924C>A (TTN)	XP_016860310.1:p.Val30308=
XM_017004822.1:c.87966C>A (TTN)	XP_016860311.1:p.Val29322=
XM_017004823.1:c.69582C>A (TTN)	XP_016860312.1:p.Val23194=
XM_024453094.1:c.91077C>A (TTN)	XP_024308862.1:p.Val30359=
XM_024453095.1:c.91074C>A (TTN)	XP_024308863.1:p.Val30358=
XM_024453096.1:c.90507C>A (TTN)	XP_024308864.1:p.Val30169=
XM_024453097.1:c.87849C>A (TTN)	XP_024308865.1:p.Val29283=
XM_024453098.1:c.87768C>A (TTN)	XP_024308866.1:p.Val29256=
XM_024453099.1:c.69531C>A (TTN)	XP_024308867.1:p.Val23177=
XM_024453100.1:c.59385C>A (TTN)	XP_024308868.1:p.Val19795=