Canonical Allele Identifier: CA3097508684
Community Standard Title: NM_001267550.2(TTN):c.41325A= (p.Val13775=)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178636402T= , CM000664.2:g.178636402T= GRCh38
NC_000002.11:g.179501129T= , CM000664.1:g.179501129T= GRCh37
NC_000002.10:g.179209374T= NCBI36
NG_011618.3:g.199401A= , LRG_391:g.199401A=

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.41325A= MANE Select NP_001254479.2:p.Val13775=
ENST00000589042.5:c.41325A= MANE Select ENSP00000467141.1:p.Val13775=
NM_001256850.1:c.36402A= NP_001243779.1:p.Val12134=
NM_003319.4:c.14130A= NP_003310.4:p.Val4710=
NM_133378.4:c.33621A= NP_596869.4:p.Val11207=
NM_133432.3:c.14505A= NP_597676.3:p.Val4835=
NM_133437.4:c.14706A= NP_597681.4:p.Val4902=
ENST00000342175.10:c.14706A= ENSP00000340554.6:p.Val4902=
ENST00000342175.11:c.14706A= ENSP00000340554.6:p.Val4902=
ENST00000342992.10:c.33621A= ENSP00000343764.6:p.Val11207=
ENST00000342992.11:c.33621A= ENSP00000343764.6:p.Val11207=
ENST00000359218.10:c.14505A= ENSP00000352154.5:p.Val4835=
ENST00000359218.9:c.14505A= ENSP00000352154.5:p.Val4835=
ENST00000460472.6:c.14130A= ENSP00000434586.1:p.Val4710=
ENST00000591111.5:c.36402A= ENSP00000465570.1:p.Val12134=
ENST00000615779.4:c.36402A= ENSP00000483597.1:p.Val12134=
XM_011511729.1:c.40422A= XP_011510031.1:p.Val13474=
XM_011511730.1:c.14316A= XP_011510032.1:p.Val4772=
XM_011511731.1:c.14175A= XP_011510033.1:p.Val4725=
XM_017004819.1:c.40218A= XP_016860308.1:p.Val13406=
XM_017004820.1:c.35616A= XP_016860309.1:p.Val11872=
XM_017004821.1:c.35613A= XP_016860310.1:p.Val11871=
XM_017004822.1:c.32655A= XP_016860311.1:p.Val10885=
XM_017004823.1:c.14271A= XP_016860312.1:p.Val4757=
XM_024453094.1:c.35766A= XP_024308862.1:p.Val11922=
XM_024453095.1:c.35763A= XP_024308863.1:p.Val11921=
XM_024453096.1:c.35196A= XP_024308864.1:p.Val11732=
XM_024453097.1:c.32538A= XP_024308865.1:p.Val10846=
XM_024453098.1:c.32457A= XP_024308866.1:p.Val10819=
XM_024453099.1:c.14220A= XP_024308867.1:p.Val4740=
XM_024453100.1:c.4074A= XP_024308868.1:p.Val1358=