Canonical Allele Identifier: CA10581868
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178620310T>C , CM000664.2:g.178620310T>C GRCh38
NC_000002.11:g.179485037T>C , CM000664.1:g.179485037T>C GRCh37
NC_000002.10:g.179193282T>C NCBI36
NG_011618.3:g.215493A>G , LRG_391:g.215493A>G
NG_051363.1:g.102484T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.38507A>G ENSP00000343764.6:p.Glu12836Gly
ENST00000342175.11:c.19592A>G ENSP00000340554.6:p.Glu6531Gly
ENST00000359218.10:c.19391A>G ENSP00000352154.5:p.Glu6464Gly
ENST00000342175.10:c.19592A>G ENSP00000340554.6:p.Glu6531Gly
ENST00000342992.10:c.38507A>G ENSP00000343764.6:p.Glu12836Gly
ENST00000359218.9:c.19391A>G ENSP00000352154.5:p.Glu6464Gly
ENST00000460472.6:c.19016A>G ENSP00000434586.1:p.Glu6339Gly
ENST00000589042.5:c.46211A>G MANE Select ENSP00000467141.1:p.Glu15404Gly
ENST00000591111.5:c.41288A>G ENSP00000465570.1:p.Glu13763Gly
ENST00000615779.4:c.41288A>G ENSP00000483597.1:p.Glu13763Gly
NM_001256850.1:c.41288A>G NP_001243779.1:p.Glu13763Gly
NM_001267550.2:c.46211A>G MANE Select NP_001254479.2:p.Glu15404Gly
NM_003319.4:c.19016A>G NP_003310.4:p.Glu6339Gly
NM_133378.4:c.38507A>G NP_596869.4:p.Glu12836Gly
NM_133432.3:c.19391A>G NP_597676.3:p.Glu6464Gly
NM_133437.4:c.19592A>G NP_597681.4:p.Glu6531Gly
XM_011511729.1:c.45308A>G XP_011510031.1:p.Glu15103Gly
XM_011511730.1:c.19202A>G XP_011510032.1:p.Glu6401Gly
XM_011511731.1:c.19061A>G XP_011510033.1:p.Glu6354Gly
XM_017004819.1:c.45104A>G XP_016860308.1:p.Glu15035Gly
XM_017004820.1:c.40502A>G XP_016860309.1:p.Glu13501Gly
XM_017004821.1:c.40499A>G XP_016860310.1:p.Glu13500Gly
XM_017004822.1:c.37541A>G XP_016860311.1:p.Glu12514Gly
XM_017004823.1:c.19157A>G XP_016860312.1:p.Glu6386Gly
XM_024453094.1:c.40652A>G XP_024308862.1:p.Glu13551Gly
XM_024453095.1:c.40649A>G XP_024308863.1:p.Glu13550Gly
XM_024453096.1:c.40082A>G XP_024308864.1:p.Glu13361Gly
XM_024453097.1:c.37424A>G XP_024308865.1:p.Glu12475Gly
XM_024453098.1:c.37343A>G XP_024308866.1:p.Glu12448Gly
XM_024453099.1:c.19106A>G XP_024308867.1:p.Glu6369Gly
XM_024453100.1:c.8960A>G XP_024308868.1:p.Glu2987Gly