Canonical Allele Identifier: CA349645541
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630314A>C , CM000664.2:g.178630314A>C GRCh38
NC_000002.11:g.179495041A>C , CM000664.1:g.179495041A>C GRCh37
NC_000002.10:g.179203286A>C NCBI36
NG_011618.3:g.205489T>G , LRG_391:g.205489T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36504T>G ENSP00000343764.6:p.Cys12168Trp
ENST00000342175.11:c.17589T>G ENSP00000340554.6:p.Cys5863Trp
ENST00000359218.10:c.17388T>G ENSP00000352154.5:p.Cys5796Trp
ENST00000342175.10:c.17589T>G ENSP00000340554.6:p.Cys5863Trp
ENST00000342992.10:c.36504T>G ENSP00000343764.6:p.Cys12168Trp
ENST00000359218.9:c.17388T>G ENSP00000352154.5:p.Cys5796Trp
ENST00000460472.6:c.17013T>G ENSP00000434586.1:p.Cys5671Trp
ENST00000589042.5:c.44208T>G MANE Select ENSP00000467141.1:p.Cys14736Trp
ENST00000591111.5:c.39285T>G ENSP00000465570.1:p.Cys13095Trp
ENST00000615779.4:c.39285T>G ENSP00000483597.1:p.Cys13095Trp
NM_001256850.1:c.39285T>G NP_001243779.1:p.Cys13095Trp
NM_001267550.2:c.44208T>G MANE Select NP_001254479.2:p.Cys14736Trp
NM_003319.4:c.17013T>G NP_003310.4:p.Cys5671Trp
NM_133378.4:c.36504T>G NP_596869.4:p.Cys12168Trp
NM_133432.3:c.17388T>G NP_597676.3:p.Cys5796Trp
NM_133437.4:c.17589T>G NP_597681.4:p.Cys5863Trp
XM_011511729.1:c.43305T>G XP_011510031.1:p.Cys14435Trp
XM_011511730.1:c.17199T>G XP_011510032.1:p.Cys5733Trp
XM_011511731.1:c.17058T>G XP_011510033.1:p.Cys5686Trp
XM_017004819.1:c.43101T>G XP_016860308.1:p.Cys14367Trp
XM_017004820.1:c.38499T>G XP_016860309.1:p.Cys12833Trp
XM_017004821.1:c.38496T>G XP_016860310.1:p.Cys12832Trp
XM_017004822.1:c.35538T>G XP_016860311.1:p.Cys11846Trp
XM_017004823.1:c.17154T>G XP_016860312.1:p.Cys5718Trp
XM_024453094.1:c.38649T>G XP_024308862.1:p.Cys12883Trp
XM_024453095.1:c.38646T>G XP_024308863.1:p.Cys12882Trp
XM_024453096.1:c.38079T>G XP_024308864.1:p.Cys12693Trp
XM_024453097.1:c.35421T>G XP_024308865.1:p.Cys11807Trp
XM_024453098.1:c.35340T>G XP_024308866.1:p.Cys11780Trp
XM_024453099.1:c.17103T>G XP_024308867.1:p.Cys5701Trp
XM_024453100.1:c.6957T>G XP_024308868.1:p.Cys2319Trp