Canonical Allele Identifier: CA349400203

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179392334G>T (hg19) ; chr2:g.178527607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527607G>T , CM000664.2:g.178527607G>T	GRCh38
NC_000002.11:g.179392334G>T , CM000664.1:g.179392334G>T	GRCh37
NC_000002.10:g.179100580G>T	NCBI36
NG_011618.3:g.308196C>A , LRG_391:g.308196C>A
NG_051363.1:g.9781G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99815C>A (TTN)	ENSP00000343764.6:p.Ala33272Asp
ENST00000342175.11:c.80900C>A (TTN)	ENSP00000340554.6:p.Ala26967Asp
ENST00000359218.10:c.80699C>A (TTN)	ENSP00000352154.5:p.Ala26900Asp
ENST00000342175.10:c.80900C>A (TTN)	ENSP00000340554.6:p.Ala26967Asp
ENST00000342992.10:c.99815C>A (TTN)	ENSP00000343764.6:p.Ala33272Asp
ENST00000359218.9:c.80699C>A (TTN)	ENSP00000352154.5:p.Ala26900Asp
ENST00000460472.6:c.80324C>A (TTN)	ENSP00000434586.1:p.Ala26775Asp
ENST00000589042.5:c.107519C>A (TTN) MANE Select	ENSP00000467141.1:p.Ala35840Asp
ENST00000591111.5:c.102596C>A (TTN)	ENSP00000465570.1:p.Ala34199Asp
ENST00000615779.4:c.102596C>A (TTN)	ENSP00000483597.1:p.Ala34199Asp
NM_001256850.1:c.102596C>A (TTN)	NP_001243779.1:p.Ala34199Asp
NM_001267550.2:c.107519C>A (TTN) MANE Select	NP_001254479.2:p.Ala35840Asp
NM_003319.4:c.80324C>A (TTN)	NP_003310.4:p.Ala26775Asp
NM_133378.4:c.99815C>A (TTN)	NP_596869.4:p.Ala33272Asp
NM_133432.3:c.80699C>A (TTN)	NP_597676.3:p.Ala26900Asp
NM_133437.4:c.80900C>A (TTN)	NP_597681.4:p.Ala26967Asp
NR_038271.1:n.446+3971G>T (TTN-AS1)
NR_038272.1:n.219+3971G>T (TTN-AS1)
XM_011511729.1:c.106616C>A (TTN)	XP_011510031.1:p.Ala35539Asp
XM_011511730.1:c.80510C>A (TTN)	XP_011510032.1:p.Ala26837Asp
XM_011511731.1:c.80369C>A (TTN)	XP_011510033.1:p.Ala26790Asp
XM_017004819.1:c.106412C>A (TTN)	XP_016860308.1:p.Ala35471Asp
XM_017004820.1:c.101810C>A (TTN)	XP_016860309.1:p.Ala33937Asp
XM_017004821.1:c.101807C>A (TTN)	XP_016860310.1:p.Ala33936Asp
XM_017004822.1:c.98849C>A (TTN)	XP_016860311.1:p.Ala32950Asp
XM_017004823.1:c.80465C>A (TTN)	XP_016860312.1:p.Ala26822Asp
XM_024453094.1:c.101960C>A (TTN)	XP_024308862.1:p.Ala33987Asp
XM_024453095.1:c.101957C>A (TTN)	XP_024308863.1:p.Ala33986Asp
XM_024453096.1:c.101390C>A (TTN)	XP_024308864.1:p.Ala33797Asp
XM_024453097.1:c.98732C>A (TTN)	XP_024308865.1:p.Ala32911Asp
XM_024453098.1:c.98651C>A (TTN)	XP_024308866.1:p.Ala32884Asp
XM_024453099.1:c.80414C>A (TTN)	XP_024308867.1:p.Ala26805Asp
XM_024453100.1:c.70268C>A (TTN)	XP_024308868.1:p.Ala23423Asp