Canonical Allele Identifier: CA430241728

Linked Data

MyVariant Identifiers: chr2:g.179409052A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178544325A>T , CM000664.2:g.178544325A>T GRCh38
NC_000002.11:g.179409052A>T , CM000664.1:g.179409052A>T GRCh37
NC_000002.10:g.179117298A>T NCBI36
NG_011618.3:g.291478T>A , LRG_391:g.291478T>A
NG_051363.1:g.26499A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.88200T>A (TTN) ENSP00000343764.6:p.Thr29400=
ENST00000342175.11:c.69285T>A (TTN) ENSP00000340554.6:p.Thr23095=
ENST00000359218.10:c.69084T>A (TTN) ENSP00000352154.5:p.Thr23028=
ENST00000342175.10:c.69285T>A (TTN) ENSP00000340554.6:p.Thr23095=
ENST00000342992.10:c.88200T>A (TTN) ENSP00000343764.6:p.Thr29400=
ENST00000359218.9:c.69084T>A (TTN) ENSP00000352154.5:p.Thr23028=
ENST00000460472.6:c.68709T>A (TTN) ENSP00000434586.1:p.Thr22903=
ENST00000589042.5:c.95904T>A (TTN) MANE Select ENSP00000467141.1:p.Thr31968=
ENST00000591111.5:c.90981T>A (TTN) ENSP00000465570.1:p.Thr30327=
ENST00000615779.4:c.90981T>A (TTN) ENSP00000483597.1:p.Thr30327=
NM_001256850.1:c.90981T>A (TTN) NP_001243779.1:p.Thr30327=
NM_001267550.2:c.95904T>A (TTN) MANE Select NP_001254479.2:p.Thr31968=
NM_003319.4:c.68709T>A (TTN) NP_003310.4:p.Thr22903=
NM_133378.4:c.88200T>A (TTN) NP_596869.4:p.Thr29400=
NM_133432.3:c.69084T>A (TTN) NP_597676.3:p.Thr23028=
NM_133437.4:c.69285T>A (TTN) NP_597681.4:p.Thr23095=
NR_038271.1:n.446+20689A>T (TTN-AS1)
NR_038272.1:n.2043+1964A>T (TTN-AS1)
XM_011511729.1:c.95001T>A (TTN) XP_011510031.1:p.Thr31667=
XM_011511730.1:c.68895T>A (TTN) XP_011510032.1:p.Thr22965=
XM_011511731.1:c.68754T>A (TTN) XP_011510033.1:p.Thr22918=
XM_017004819.1:c.94797T>A (TTN) XP_016860308.1:p.Thr31599=
XM_017004820.1:c.90195T>A (TTN) XP_016860309.1:p.Thr30065=
XM_017004821.1:c.90192T>A (TTN) XP_016860310.1:p.Thr30064=
XM_017004822.1:c.87234T>A (TTN) XP_016860311.1:p.Thr29078=
XM_017004823.1:c.68850T>A (TTN) XP_016860312.1:p.Thr22950=
XM_024453094.1:c.90345T>A (TTN) XP_024308862.1:p.Thr30115=
XM_024453095.1:c.90342T>A (TTN) XP_024308863.1:p.Thr30114=
XM_024453096.1:c.89775T>A (TTN) XP_024308864.1:p.Thr29925=
XM_024453097.1:c.87117T>A (TTN) XP_024308865.1:p.Thr29039=
XM_024453098.1:c.87036T>A (TTN) XP_024308866.1:p.Thr29012=
XM_024453099.1:c.68799T>A (TTN) XP_024308867.1:p.Thr22933=
XM_024453100.1:c.58653T>A (TTN) XP_024308868.1:p.Thr19551=