Canonical Allele Identifier: CA349407199

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395318A>C (hg19) ; chr2:g.178530591A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530591A>C , CM000664.2:g.178530591A>C	GRCh38
NC_000002.11:g.179395318A>C , CM000664.1:g.179395318A>C	GRCh37
NC_000002.10:g.179103564A>C	NCBI36
NG_011618.3:g.305212T>G , LRG_391:g.305212T>G
NG_051363.1:g.12765A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98320T>G (TTN)	ENSP00000343764.6:p.Tyr32774Asp
ENST00000342175.11:c.79405T>G (TTN)	ENSP00000340554.6:p.Tyr26469Asp
ENST00000359218.10:c.79204T>G (TTN)	ENSP00000352154.5:p.Tyr26402Asp
ENST00000342175.10:c.79405T>G (TTN)	ENSP00000340554.6:p.Tyr26469Asp
ENST00000342992.10:c.98320T>G (TTN)	ENSP00000343764.6:p.Tyr32774Asp
ENST00000359218.9:c.79204T>G (TTN)	ENSP00000352154.5:p.Tyr26402Asp
ENST00000460472.6:c.78829T>G (TTN)	ENSP00000434586.1:p.Tyr26277Asp
ENST00000589042.5:c.106024T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr35342Asp
ENST00000591111.5:c.101101T>G (TTN)	ENSP00000465570.1:p.Tyr33701Asp
ENST00000615779.4:c.101101T>G (TTN)	ENSP00000483597.1:p.Tyr33701Asp
NM_001256850.1:c.101101T>G (TTN)	NP_001243779.1:p.Tyr33701Asp
NM_001267550.2:c.106024T>G (TTN) MANE Select	NP_001254479.2:p.Tyr35342Asp
NM_003319.4:c.78829T>G (TTN)	NP_003310.4:p.Tyr26277Asp
NM_133378.4:c.98320T>G (TTN)	NP_596869.4:p.Tyr32774Asp
NM_133432.3:c.79204T>G (TTN)	NP_597676.3:p.Tyr26402Asp
NM_133437.4:c.79405T>G (TTN)	NP_597681.4:p.Tyr26469Asp
NR_038271.1:n.446+6955A>C (TTN-AS1)
NR_038272.1:n.220-5141A>C (TTN-AS1)
XM_011511729.1:c.105121T>G (TTN)	XP_011510031.1:p.Tyr35041Asp
XM_011511730.1:c.79015T>G (TTN)	XP_011510032.1:p.Tyr26339Asp
XM_011511731.1:c.78874T>G (TTN)	XP_011510033.1:p.Tyr26292Asp
XM_017004819.1:c.104917T>G (TTN)	XP_016860308.1:p.Tyr34973Asp
XM_017004820.1:c.100315T>G (TTN)	XP_016860309.1:p.Tyr33439Asp
XM_017004821.1:c.100312T>G (TTN)	XP_016860310.1:p.Tyr33438Asp
XM_017004822.1:c.97354T>G (TTN)	XP_016860311.1:p.Tyr32452Asp
XM_017004823.1:c.78970T>G (TTN)	XP_016860312.1:p.Tyr26324Asp
XM_024453094.1:c.100465T>G (TTN)	XP_024308862.1:p.Tyr33489Asp
XM_024453095.1:c.100462T>G (TTN)	XP_024308863.1:p.Tyr33488Asp
XM_024453096.1:c.99895T>G (TTN)	XP_024308864.1:p.Tyr33299Asp
XM_024453097.1:c.97237T>G (TTN)	XP_024308865.1:p.Tyr32413Asp
XM_024453098.1:c.97156T>G (TTN)	XP_024308866.1:p.Tyr32386Asp
XM_024453099.1:c.78919T>G (TTN)	XP_024308867.1:p.Tyr26307Asp
XM_024453100.1:c.68773T>G (TTN)	XP_024308868.1:p.Tyr22925Asp