Canonical Allele Identifier: CA1310518067

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532080T= , CM000664.2:g.178532080T= GRCh38
NC_000002.11:g.179396807T= , CM000664.1:g.179396807T= GRCh37
NC_000002.10:g.179105053T= NCBI36
NG_011618.3:g.303723A= , LRG_391:g.303723A=
NG_051363.1:g.14254T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96831A= (TTN) ENSP00000343764.6:p.Pro32277=
ENST00000342175.11:c.77916A= (TTN) ENSP00000340554.6:p.Pro25972=
ENST00000359218.10:c.77715A= (TTN) ENSP00000352154.5:p.Pro25905=
ENST00000342175.10:c.77916A= (TTN) ENSP00000340554.6:p.Pro25972=
ENST00000342992.10:c.96831A= (TTN) ENSP00000343764.6:p.Pro32277=
ENST00000359218.9:c.77715A= (TTN) ENSP00000352154.5:p.Pro25905=
ENST00000460472.6:c.77340A= (TTN) ENSP00000434586.1:p.Pro25780=
ENST00000589042.5:c.104535A= (TTN) MANE Select ENSP00000467141.1:p.Pro34845=
ENST00000591111.5:c.99612A= (TTN) ENSP00000465570.1:p.Pro33204=
ENST00000615779.4:c.99612A= (TTN) ENSP00000483597.1:p.Pro33204=
NM_001256850.1:c.99612A= (TTN) NP_001243779.1:p.Pro33204=
NM_001267550.2:c.104535A= (TTN) MANE Select NP_001254479.2:p.Pro34845=
NM_003319.4:c.77340A= (TTN) NP_003310.4:p.Pro25780=
NM_133378.4:c.96831A= (TTN) NP_596869.4:p.Pro32277=
NM_133432.3:c.77715A= (TTN) NP_597676.3:p.Pro25905=
NM_133437.4:c.77916A= (TTN) NP_597681.4:p.Pro25972=
NR_038271.1:n.446+8444T= (TTN-AS1)
NR_038272.1:n.220-3652T= (TTN-AS1)
XM_011511729.1:c.103632A= (TTN) XP_011510031.1:p.Pro34544=
XM_011511730.1:c.77526A= (TTN) XP_011510032.1:p.Pro25842=
XM_011511731.1:c.77385A= (TTN) XP_011510033.1:p.Pro25795=
XM_017004819.1:c.103428A= (TTN) XP_016860308.1:p.Pro34476=
XM_017004820.1:c.98826A= (TTN) XP_016860309.1:p.Pro32942=
XM_017004821.1:c.98823A= (TTN) XP_016860310.1:p.Pro32941=
XM_017004822.1:c.95865A= (TTN) XP_016860311.1:p.Pro31955=
XM_017004823.1:c.77481A= (TTN) XP_016860312.1:p.Pro25827=
XM_024453094.1:c.98976A= (TTN) XP_024308862.1:p.Pro32992=
XM_024453095.1:c.98973A= (TTN) XP_024308863.1:p.Pro32991=
XM_024453096.1:c.98406A= (TTN) XP_024308864.1:p.Pro32802=
XM_024453097.1:c.95748A= (TTN) XP_024308865.1:p.Pro31916=
XM_024453098.1:c.95667A= (TTN) XP_024308866.1:p.Pro31889=
XM_024453099.1:c.77430A= (TTN) XP_024308867.1:p.Pro25810=
XM_024453100.1:c.67284A= (TTN) XP_024308868.1:p.Pro22428=