Canonical Allele Identifier: CA430114694

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501441T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636714T>C , CM000664.2:g.178636714T>C	GRCh38
NC_000002.11:g.179501441T>C , CM000664.1:g.179501441T>C	GRCh37
NC_000002.10:g.179209686T>C	NCBI36
NG_011618.3:g.199089A>G , LRG_391:g.199089A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33309A>G	ENSP00000343764.6:p.Glu11103=
ENST00000342175.11:c.14394A>G	ENSP00000340554.6:p.Glu4798=
ENST00000359218.10:c.14193A>G	ENSP00000352154.5:p.Glu4731=
ENST00000342175.10:c.14394A>G	ENSP00000340554.6:p.Glu4798=
ENST00000342992.10:c.33309A>G	ENSP00000343764.6:p.Glu11103=
ENST00000359218.9:c.14193A>G	ENSP00000352154.5:p.Glu4731=
ENST00000460472.6:c.13818A>G	ENSP00000434586.1:p.Glu4606=
ENST00000589042.5:c.41013A>G MANE Select	ENSP00000467141.1:p.Glu13671=
ENST00000591111.5:c.36090A>G	ENSP00000465570.1:p.Glu12030=
ENST00000615779.4:c.36090A>G	ENSP00000483597.1:p.Glu12030=
NM_001256850.1:c.36090A>G	NP_001243779.1:p.Glu12030=
NM_001267550.2:c.41013A>G MANE Select	NP_001254479.2:p.Glu13671=
NM_003319.4:c.13818A>G	NP_003310.4:p.Glu4606=
NM_133378.4:c.33309A>G	NP_596869.4:p.Glu11103=
NM_133432.3:c.14193A>G	NP_597676.3:p.Glu4731=
NM_133437.4:c.14394A>G	NP_597681.4:p.Glu4798=
XM_011511729.1:c.40110A>G	XP_011510031.1:p.Glu13370=
XM_011511730.1:c.14004A>G	XP_011510032.1:p.Glu4668=
XM_011511731.1:c.13863A>G	XP_011510033.1:p.Glu4621=
XM_017004819.1:c.39906A>G	XP_016860308.1:p.Glu13302=
XM_017004820.1:c.35304A>G	XP_016860309.1:p.Glu11768=
XM_017004821.1:c.35301A>G	XP_016860310.1:p.Glu11767=
XM_017004822.1:c.32343A>G	XP_016860311.1:p.Glu10781=
XM_017004823.1:c.13959A>G	XP_016860312.1:p.Glu4653=
XM_024453094.1:c.35454A>G	XP_024308862.1:p.Glu11818=
XM_024453095.1:c.35451A>G	XP_024308863.1:p.Glu11817=
XM_024453096.1:c.34884A>G	XP_024308864.1:p.Glu11628=
XM_024453097.1:c.32226A>G	XP_024308865.1:p.Glu10742=
XM_024453098.1:c.32145A>G	XP_024308866.1:p.Glu10715=
XM_024453099.1:c.13908A>G	XP_024308867.1:p.Glu4636=
XM_024453100.1:c.3762A>G	XP_024308868.1:p.Glu1254=