Canonical Allele Identifier: CA430267853

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179457785A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178593058A>T , CM000664.2:g.178593058A>T	GRCh38
NC_000002.11:g.179457785A>T , CM000664.1:g.179457785A>T	GRCh37
NC_000002.10:g.179166031A>T	NCBI36
NG_011618.3:g.242745T>A , LRG_391:g.242745T>A
NG_051363.1:g.75232A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51357T>A (TTN)	ENSP00000343764.6:p.Pro17119=
ENST00000342175.11:c.32442T>A (TTN)	ENSP00000340554.6:p.Pro10814=
ENST00000359218.10:c.32241T>A (TTN)	ENSP00000352154.5:p.Pro10747=
ENST00000342175.10:c.32442T>A (TTN)	ENSP00000340554.6:p.Pro10814=
ENST00000342992.10:c.51357T>A (TTN)	ENSP00000343764.6:p.Pro17119=
ENST00000359218.9:c.32241T>A (TTN)	ENSP00000352154.5:p.Pro10747=
ENST00000460472.6:c.31866T>A (TTN)	ENSP00000434586.1:p.Pro10622=
ENST00000589042.5:c.59061T>A (TTN) MANE Select	ENSP00000467141.1:p.Pro19687=
ENST00000591111.5:c.54138T>A (TTN)	ENSP00000465570.1:p.Pro18046=
ENST00000615779.4:c.54138T>A (TTN)	ENSP00000483597.1:p.Pro18046=
NM_001256850.1:c.54138T>A (TTN)	NP_001243779.1:p.Pro18046=
NM_001267550.2:c.59061T>A (TTN) MANE Select	NP_001254479.2:p.Pro19687=
NM_003319.4:c.31866T>A (TTN)	NP_003310.4:p.Pro10622=
NM_133378.4:c.51357T>A (TTN)	NP_596869.4:p.Pro17119=
NM_133432.3:c.32241T>A (TTN)	NP_597676.3:p.Pro10747=
NM_133437.4:c.32442T>A (TTN)	NP_597681.4:p.Pro10814=
NR_038271.1:n.597-4538A>T (TTN-AS1)
NR_038272.1:n.3364+1744A>T (TTN-AS1)
XM_011511729.1:c.58158T>A (TTN)	XP_011510031.1:p.Pro19386=
XM_011511730.1:c.32052T>A (TTN)	XP_011510032.1:p.Pro10684=
XM_011511731.1:c.31911T>A (TTN)	XP_011510033.1:p.Pro10637=
XM_017004819.1:c.57954T>A (TTN)	XP_016860308.1:p.Pro19318=
XM_017004820.1:c.53352T>A (TTN)	XP_016860309.1:p.Pro17784=
XM_017004821.1:c.53349T>A (TTN)	XP_016860310.1:p.Pro17783=
XM_017004822.1:c.50391T>A (TTN)	XP_016860311.1:p.Pro16797=
XM_017004823.1:c.32007T>A (TTN)	XP_016860312.1:p.Pro10669=
XM_024453094.1:c.53502T>A (TTN)	XP_024308862.1:p.Pro17834=
XM_024453095.1:c.53499T>A (TTN)	XP_024308863.1:p.Pro17833=
XM_024453096.1:c.52932T>A (TTN)	XP_024308864.1:p.Pro17644=
XM_024453097.1:c.50274T>A (TTN)	XP_024308865.1:p.Pro16758=
XM_024453098.1:c.50193T>A (TTN)	XP_024308866.1:p.Pro16731=
XM_024453099.1:c.31956T>A (TTN)	XP_024308867.1:p.Pro10652=
XM_024453100.1:c.21810T>A (TTN)	XP_024308868.1:p.Pro7270=