Canonical Allele Identifier: CA349628924
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178620340A>C , CM000664.2:g.178620340A>C GRCh38
NC_000002.11:g.179485067A>C , CM000664.1:g.179485067A>C GRCh37
NC_000002.10:g.179193312A>C NCBI36
NG_011618.3:g.215463T>G , LRG_391:g.215463T>G
NG_051363.1:g.102514A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.38477T>G ENSP00000343764.6:p.Val12826Gly
ENST00000342175.11:c.19562T>G ENSP00000340554.6:p.Val6521Gly
ENST00000359218.10:c.19361T>G ENSP00000352154.5:p.Val6454Gly
ENST00000342175.10:c.19562T>G ENSP00000340554.6:p.Val6521Gly
ENST00000342992.10:c.38477T>G ENSP00000343764.6:p.Val12826Gly
ENST00000359218.9:c.19361T>G ENSP00000352154.5:p.Val6454Gly
ENST00000460472.6:c.18986T>G ENSP00000434586.1:p.Val6329Gly
ENST00000589042.5:c.46181T>G MANE Select ENSP00000467141.1:p.Val15394Gly
ENST00000591111.5:c.41258T>G ENSP00000465570.1:p.Val13753Gly
ENST00000615779.4:c.41258T>G ENSP00000483597.1:p.Val13753Gly
NM_001256850.1:c.41258T>G NP_001243779.1:p.Val13753Gly
NM_001267550.2:c.46181T>G MANE Select NP_001254479.2:p.Val15394Gly
NM_003319.4:c.18986T>G NP_003310.4:p.Val6329Gly
NM_133378.4:c.38477T>G NP_596869.4:p.Val12826Gly
NM_133432.3:c.19361T>G NP_597676.3:p.Val6454Gly
NM_133437.4:c.19562T>G NP_597681.4:p.Val6521Gly
XM_011511729.1:c.45278T>G XP_011510031.1:p.Val15093Gly
XM_011511730.1:c.19172T>G XP_011510032.1:p.Val6391Gly
XM_011511731.1:c.19031T>G XP_011510033.1:p.Val6344Gly
XM_017004819.1:c.45074T>G XP_016860308.1:p.Val15025Gly
XM_017004820.1:c.40472T>G XP_016860309.1:p.Val13491Gly
XM_017004821.1:c.40469T>G XP_016860310.1:p.Val13490Gly
XM_017004822.1:c.37511T>G XP_016860311.1:p.Val12504Gly
XM_017004823.1:c.19127T>G XP_016860312.1:p.Val6376Gly
XM_024453094.1:c.40622T>G XP_024308862.1:p.Val13541Gly
XM_024453095.1:c.40619T>G XP_024308863.1:p.Val13540Gly
XM_024453096.1:c.40052T>G XP_024308864.1:p.Val13351Gly
XM_024453097.1:c.37394T>G XP_024308865.1:p.Val12465Gly
XM_024453098.1:c.37313T>G XP_024308866.1:p.Val12438Gly
XM_024453099.1:c.19076T>G XP_024308867.1:p.Val6359Gly
XM_024453100.1:c.8930T>G XP_024308868.1:p.Val2977Gly