Canonical Allele Identifier: CA1310551140

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618685_178618688delinsAAAG , CM000664.2:g.178618685_178618688delinsAAAG GRCh38
NC_000002.11:g.179483412_179483415delinsAAAG , CM000664.1:g.179483412_179483415delinsAAAG GRCh37
NC_000002.10:g.179191657_179191660delinsAAAG NCBI36
NG_011618.3:g.217115_217118delinsCTTT , LRG_391:g.217115_217118delinsCTTT
NG_051363.1:g.100859_100862delinsAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39158_39161delinsCTTT (TTN) ENSP00000343764.6:p.Ser13053=
ENST00000342175.11:c.20243_20246delinsCTTT (TTN) ENSP00000340554.6:p.Ser6748=
ENST00000359218.10:c.20042_20045delinsCTTT (TTN) ENSP00000352154.5:p.Ser6681=
ENST00000342175.10:c.20243_20246delinsCTTT (TTN) ENSP00000340554.6:p.Ser6748=
ENST00000342992.10:c.39158_39161delinsCTTT (TTN) ENSP00000343764.6:p.Ser13053=
ENST00000359218.9:c.20042_20045delinsCTTT (TTN) ENSP00000352154.5:p.Ser6681=
ENST00000460472.6:c.19667_19670delinsCTTT (TTN) ENSP00000434586.1:p.Ser6556=
ENST00000589042.5:c.46862_46865delinsCTTT (TTN) MANE Select ENSP00000467141.1:p.Ser15621=
ENST00000591111.5:c.41939_41942delinsCTTT (TTN) ENSP00000465570.1:p.Ser13980=
ENST00000615779.4:c.41939_41942delinsCTTT (TTN) ENSP00000483597.1:p.Ser13980=
NM_001256850.1:c.41939_41942delinsCTTT (TTN) NP_001243779.1:p.Ser13980=
NM_001267550.2:c.46862_46865delinsCTTT (TTN) MANE Select NP_001254479.2:p.Ser15621=
NM_003319.4:c.19667_19670delinsCTTT (TTN) NP_003310.4:p.Ser6556=
NM_133378.4:c.39158_39161delinsCTTT (TTN) NP_596869.4:p.Ser13053=
NM_133432.3:c.20042_20045delinsCTTT (TTN) NP_597676.3:p.Ser6681=
NM_133437.4:c.20243_20246delinsCTTT (TTN) NP_597681.4:p.Ser6748=
NR_038271.1:n.1605-1068_1605-1065delinsAAAG (TTN-AS1)
XM_011511729.1:c.45959_45962delinsCTTT (TTN) XP_011510031.1:p.Ser15320=
XM_011511730.1:c.19853_19856delinsCTTT (TTN) XP_011510032.1:p.Ser6618=
XM_011511731.1:c.19712_19715delinsCTTT (TTN) XP_011510033.1:p.Ser6571=
XM_017004819.1:c.45755_45758delinsCTTT (TTN) XP_016860308.1:p.Ser15252=
XM_017004820.1:c.41153_41156delinsCTTT (TTN) XP_016860309.1:p.Ser13718=
XM_017004821.1:c.41150_41153delinsCTTT (TTN) XP_016860310.1:p.Ser13717=
XM_017004822.1:c.38192_38195delinsCTTT (TTN) XP_016860311.1:p.Ser12731=
XM_017004823.1:c.19808_19811delinsCTTT (TTN) XP_016860312.1:p.Ser6603=
XM_024453094.1:c.41303_41306delinsCTTT (TTN) XP_024308862.1:p.Ser13768=
XM_024453095.1:c.41300_41303delinsCTTT (TTN) XP_024308863.1:p.Ser13767=
XM_024453096.1:c.40733_40736delinsCTTT (TTN) XP_024308864.1:p.Ser13578=
XM_024453097.1:c.38075_38078delinsCTTT (TTN) XP_024308865.1:p.Ser12692=
XM_024453098.1:c.37994_37997delinsCTTT (TTN) XP_024308866.1:p.Ser12665=
XM_024453099.1:c.19757_19760delinsCTTT (TTN) XP_024308867.1:p.Ser6586=
XM_024453100.1:c.9611_9614delinsCTTT (TTN) XP_024308868.1:p.Ser3204=