Canonical Allele Identifier: CA349407194

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395316A>T (hg19) ; chr2:g.178530589A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530589A>T , CM000664.2:g.178530589A>T	GRCh38
NC_000002.11:g.179395316A>T , CM000664.1:g.179395316A>T	GRCh37
NC_000002.10:g.179103562A>T	NCBI36
NG_011618.3:g.305214T>A , LRG_391:g.305214T>A
NG_051363.1:g.12763A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98322T>A (TTN)	ENSP00000343764.6:p.Tyr32774Ter
ENST00000342175.11:c.79407T>A (TTN)	ENSP00000340554.6:p.Tyr26469Ter
ENST00000359218.10:c.79206T>A (TTN)	ENSP00000352154.5:p.Tyr26402Ter
ENST00000342175.10:c.79407T>A (TTN)	ENSP00000340554.6:p.Tyr26469Ter
ENST00000342992.10:c.98322T>A (TTN)	ENSP00000343764.6:p.Tyr32774Ter
ENST00000359218.9:c.79206T>A (TTN)	ENSP00000352154.5:p.Tyr26402Ter
ENST00000460472.6:c.78831T>A (TTN)	ENSP00000434586.1:p.Tyr26277Ter
ENST00000589042.5:c.106026T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr35342Ter
ENST00000591111.5:c.101103T>A (TTN)	ENSP00000465570.1:p.Tyr33701Ter
ENST00000615779.4:c.101103T>A (TTN)	ENSP00000483597.1:p.Tyr33701Ter
NM_001256850.1:c.101103T>A (TTN)	NP_001243779.1:p.Tyr33701Ter
NM_001267550.2:c.106026T>A (TTN) MANE Select	NP_001254479.2:p.Tyr35342Ter
NM_003319.4:c.78831T>A (TTN)	NP_003310.4:p.Tyr26277Ter
NM_133378.4:c.98322T>A (TTN)	NP_596869.4:p.Tyr32774Ter
NM_133432.3:c.79206T>A (TTN)	NP_597676.3:p.Tyr26402Ter
NM_133437.4:c.79407T>A (TTN)	NP_597681.4:p.Tyr26469Ter
NR_038271.1:n.446+6953A>T (TTN-AS1)
NR_038272.1:n.220-5143A>T (TTN-AS1)
XM_011511729.1:c.105123T>A (TTN)	XP_011510031.1:p.Tyr35041Ter
XM_011511730.1:c.79017T>A (TTN)	XP_011510032.1:p.Tyr26339Ter
XM_011511731.1:c.78876T>A (TTN)	XP_011510033.1:p.Tyr26292Ter
XM_017004819.1:c.104919T>A (TTN)	XP_016860308.1:p.Tyr34973Ter
XM_017004820.1:c.100317T>A (TTN)	XP_016860309.1:p.Tyr33439Ter
XM_017004821.1:c.100314T>A (TTN)	XP_016860310.1:p.Tyr33438Ter
XM_017004822.1:c.97356T>A (TTN)	XP_016860311.1:p.Tyr32452Ter
XM_017004823.1:c.78972T>A (TTN)	XP_016860312.1:p.Tyr26324Ter
XM_024453094.1:c.100467T>A (TTN)	XP_024308862.1:p.Tyr33489Ter
XM_024453095.1:c.100464T>A (TTN)	XP_024308863.1:p.Tyr33488Ter
XM_024453096.1:c.99897T>A (TTN)	XP_024308864.1:p.Tyr33299Ter
XM_024453097.1:c.97239T>A (TTN)	XP_024308865.1:p.Tyr32413Ter
XM_024453098.1:c.97158T>A (TTN)	XP_024308866.1:p.Tyr32386Ter
XM_024453099.1:c.78921T>A (TTN)	XP_024308867.1:p.Tyr26307Ter
XM_024453100.1:c.68775T>A (TTN)	XP_024308868.1:p.Tyr22925Ter