Canonical Allele Identifier: CA349405527

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394820A>T (hg19) ; chr2:g.178530093A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530093A>T , CM000664.2:g.178530093A>T	GRCh38
NC_000002.11:g.179394820A>T , CM000664.1:g.179394820A>T	GRCh37
NC_000002.10:g.179103066A>T	NCBI36
NG_011618.3:g.305710T>A , LRG_391:g.305710T>A
NG_051363.1:g.12267A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98694T>A (TTN)	ENSP00000343764.6:p.Tyr32898Ter
ENST00000342175.11:c.79779T>A (TTN)	ENSP00000340554.6:p.Tyr26593Ter
ENST00000359218.10:c.79578T>A (TTN)	ENSP00000352154.5:p.Tyr26526Ter
ENST00000342175.10:c.79779T>A (TTN)	ENSP00000340554.6:p.Tyr26593Ter
ENST00000342992.10:c.98694T>A (TTN)	ENSP00000343764.6:p.Tyr32898Ter
ENST00000359218.9:c.79578T>A (TTN)	ENSP00000352154.5:p.Tyr26526Ter
ENST00000460472.6:c.79203T>A (TTN)	ENSP00000434586.1:p.Tyr26401Ter
ENST00000589042.5:c.106398T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr35466Ter
ENST00000591111.5:c.101475T>A (TTN)	ENSP00000465570.1:p.Tyr33825Ter
ENST00000615779.4:c.101475T>A (TTN)	ENSP00000483597.1:p.Tyr33825Ter
NM_001256850.1:c.101475T>A (TTN)	NP_001243779.1:p.Tyr33825Ter
NM_001267550.2:c.106398T>A (TTN) MANE Select	NP_001254479.2:p.Tyr35466Ter
NM_003319.4:c.79203T>A (TTN)	NP_003310.4:p.Tyr26401Ter
NM_133378.4:c.98694T>A (TTN)	NP_596869.4:p.Tyr32898Ter
NM_133432.3:c.79578T>A (TTN)	NP_597676.3:p.Tyr26526Ter
NM_133437.4:c.79779T>A (TTN)	NP_597681.4:p.Tyr26593Ter
NR_038271.1:n.446+6457A>T (TTN-AS1)
NR_038272.1:n.220-5639A>T (TTN-AS1)
XM_011511729.1:c.105495T>A (TTN)	XP_011510031.1:p.Tyr35165Ter
XM_011511730.1:c.79389T>A (TTN)	XP_011510032.1:p.Tyr26463Ter
XM_011511731.1:c.79248T>A (TTN)	XP_011510033.1:p.Tyr26416Ter
XM_017004819.1:c.105291T>A (TTN)	XP_016860308.1:p.Tyr35097Ter
XM_017004820.1:c.100689T>A (TTN)	XP_016860309.1:p.Tyr33563Ter
XM_017004821.1:c.100686T>A (TTN)	XP_016860310.1:p.Tyr33562Ter
XM_017004822.1:c.97728T>A (TTN)	XP_016860311.1:p.Tyr32576Ter
XM_017004823.1:c.79344T>A (TTN)	XP_016860312.1:p.Tyr26448Ter
XM_024453094.1:c.100839T>A (TTN)	XP_024308862.1:p.Tyr33613Ter
XM_024453095.1:c.100836T>A (TTN)	XP_024308863.1:p.Tyr33612Ter
XM_024453096.1:c.100269T>A (TTN)	XP_024308864.1:p.Tyr33423Ter
XM_024453097.1:c.97611T>A (TTN)	XP_024308865.1:p.Tyr32537Ter
XM_024453098.1:c.97530T>A (TTN)	XP_024308866.1:p.Tyr32510Ter
XM_024453099.1:c.79293T>A (TTN)	XP_024308867.1:p.Tyr26431Ter
XM_024453100.1:c.69147T>A (TTN)	XP_024308868.1:p.Tyr23049Ter