Canonical Allele Identifier: CA430277934
Community Standard Title: NM_001267550.2(TTN):c.41328A>G (p.Glu13776=)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178636399T>C , CM000664.2:g.178636399T>C GRCh38
NC_000002.11:g.179501126T>C , CM000664.1:g.179501126T>C GRCh37
NC_000002.10:g.179209371T>C NCBI36
NG_011618.3:g.199404A>G , LRG_391:g.199404A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.41328A>G MANE Select NP_001254479.2:p.Glu13776=
ENST00000589042.5:c.41328A>G MANE Select ENSP00000467141.1:p.Glu13776=
NM_001256850.1:c.36405A>G NP_001243779.1:p.Glu12135=
NM_003319.4:c.14133A>G NP_003310.4:p.Glu4711=
NM_133378.4:c.33624A>G NP_596869.4:p.Glu11208=
NM_133432.3:c.14508A>G NP_597676.3:p.Glu4836=
NM_133437.4:c.14709A>G NP_597681.4:p.Glu4903=
ENST00000342175.10:c.14709A>G ENSP00000340554.6:p.Glu4903=
ENST00000342175.11:c.14709A>G ENSP00000340554.6:p.Glu4903=
ENST00000342992.10:c.33624A>G ENSP00000343764.6:p.Glu11208=
ENST00000342992.11:c.33624A>G ENSP00000343764.6:p.Glu11208=
ENST00000359218.10:c.14508A>G ENSP00000352154.5:p.Glu4836=
ENST00000359218.9:c.14508A>G ENSP00000352154.5:p.Glu4836=
ENST00000460472.6:c.14133A>G ENSP00000434586.1:p.Glu4711=
ENST00000591111.5:c.36405A>G ENSP00000465570.1:p.Glu12135=
ENST00000615779.4:c.36405A>G ENSP00000483597.1:p.Glu12135=
XM_011511729.1:c.40425A>G XP_011510031.1:p.Glu13475=
XM_011511730.1:c.14319A>G XP_011510032.1:p.Glu4773=
XM_011511731.1:c.14178A>G XP_011510033.1:p.Glu4726=
XM_017004819.1:c.40221A>G XP_016860308.1:p.Glu13407=
XM_017004820.1:c.35619A>G XP_016860309.1:p.Glu11873=
XM_017004821.1:c.35616A>G XP_016860310.1:p.Glu11872=
XM_017004822.1:c.32658A>G XP_016860311.1:p.Glu10886=
XM_017004823.1:c.14274A>G XP_016860312.1:p.Glu4758=
XM_024453094.1:c.35769A>G XP_024308862.1:p.Glu11923=
XM_024453095.1:c.35766A>G XP_024308863.1:p.Glu11922=
XM_024453096.1:c.35199A>G XP_024308864.1:p.Glu11733=
XM_024453097.1:c.32541A>G XP_024308865.1:p.Glu10847=
XM_024453098.1:c.32460A>G XP_024308866.1:p.Glu10820=
XM_024453099.1:c.14223A>G XP_024308867.1:p.Glu4741=
XM_024453100.1:c.4077A>G XP_024308868.1:p.Glu1359=