Canonical Allele Identifier: CA349600885

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179432012C>T (hg19) ; chr2:g.178567285C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178567285C>T , CM000664.2:g.178567285C>T	GRCh38
NC_000002.11:g.179432012C>T , CM000664.1:g.179432012C>T	GRCh37
NC_000002.10:g.179140258C>T	NCBI36
NG_011618.3:g.268518G>A , LRG_391:g.268518G>A
NG_051363.1:g.49459C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.71143G>A (TTN)	ENSP00000343764.6:p.Val23715Ile
ENST00000342175.11:c.52228G>A (TTN)	ENSP00000340554.6:p.Val17410Ile
ENST00000359218.10:c.52027G>A (TTN)	ENSP00000352154.5:p.Val17343Ile
ENST00000342175.10:c.52228G>A (TTN)	ENSP00000340554.6:p.Val17410Ile
ENST00000342992.10:c.71143G>A (TTN)	ENSP00000343764.6:p.Val23715Ile
ENST00000359218.9:c.52027G>A (TTN)	ENSP00000352154.5:p.Val17343Ile
ENST00000460472.6:c.51652G>A (TTN)	ENSP00000434586.1:p.Val17218Ile
ENST00000589042.5:c.78847G>A (TTN) MANE Select	ENSP00000467141.1:p.Val26283Ile
ENST00000591111.5:c.73924G>A (TTN)	ENSP00000465570.1:p.Val24642Ile
ENST00000615779.4:c.73924G>A (TTN)	ENSP00000483597.1:p.Val24642Ile
NM_001256850.1:c.73924G>A (TTN)	NP_001243779.1:p.Val24642Ile
NM_001267550.2:c.78847G>A (TTN) MANE Select	NP_001254479.2:p.Val26283Ile
NM_003319.4:c.51652G>A (TTN)	NP_003310.4:p.Val17218Ile
NM_133378.4:c.71143G>A (TTN)	NP_596869.4:p.Val23715Ile
NM_133432.3:c.52027G>A (TTN)	NP_597676.3:p.Val17343Ile
NM_133437.4:c.52228G>A (TTN)	NP_597681.4:p.Val17410Ile
NR_038271.1:n.447-4015C>T (TTN-AS1)
NR_038272.1:n.2044-15287C>T (TTN-AS1)
XM_011511729.1:c.77944G>A (TTN)	XP_011510031.1:p.Val25982Ile
XM_011511730.1:c.51838G>A (TTN)	XP_011510032.1:p.Val17280Ile
XM_011511731.1:c.51697G>A (TTN)	XP_011510033.1:p.Val17233Ile
XM_017004819.1:c.77740G>A (TTN)	XP_016860308.1:p.Val25914Ile
XM_017004820.1:c.73138G>A (TTN)	XP_016860309.1:p.Val24380Ile
XM_017004821.1:c.73135G>A (TTN)	XP_016860310.1:p.Val24379Ile
XM_017004822.1:c.70177G>A (TTN)	XP_016860311.1:p.Val23393Ile
XM_017004823.1:c.51793G>A (TTN)	XP_016860312.1:p.Val17265Ile
XM_024453094.1:c.73288G>A (TTN)	XP_024308862.1:p.Val24430Ile
XM_024453095.1:c.73285G>A (TTN)	XP_024308863.1:p.Val24429Ile
XM_024453096.1:c.72718G>A (TTN)	XP_024308864.1:p.Val24240Ile
XM_024453097.1:c.70060G>A (TTN)	XP_024308865.1:p.Val23354Ile
XM_024453098.1:c.69979G>A (TTN)	XP_024308866.1:p.Val23327Ile
XM_024453099.1:c.51742G>A (TTN)	XP_024308867.1:p.Val17248Ile
XM_024453100.1:c.41596G>A (TTN)	XP_024308868.1:p.Val13866Ile