Canonical Allele Identifier: CA349671442

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577763C>T , CM000664.2:g.178577763C>T	GRCh38
NC_000002.11:g.179442490C>T , CM000664.1:g.179442490C>T	GRCh37
NC_000002.10:g.179150736C>T	NCBI36
NG_011618.3:g.258040G>A , LRG_391:g.258040G>A
NG_051363.1:g.59937C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.68663G>A (TTN) MANE Select	NP_001254479.2:p.Trp22888Ter
ENST00000589042.5:c.68663G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp22888Ter
NM_001256850.1:c.63740G>A (TTN)	NP_001243779.1:p.Trp21247Ter
NM_003319.4:c.41468G>A (TTN)	NP_003310.4:p.Trp13823Ter
NM_133378.4:c.60959G>A (TTN)	NP_596869.4:p.Trp20320Ter
NM_133432.3:c.41843G>A (TTN)	NP_597676.3:p.Trp13948Ter
NM_133437.4:c.42044G>A (TTN)	NP_597681.4:p.Trp14015Ter
NR_038271.1:n.596+6314C>T (TTN-AS1)
NR_038272.1:n.2044-4809C>T (TTN-AS1)
ENST00000342175.10:c.42044G>A (TTN)	ENSP00000340554.6:p.Trp14015Ter
ENST00000342175.11:c.42044G>A (TTN)	ENSP00000340554.6:p.Trp14015Ter
ENST00000342992.10:c.60959G>A (TTN)	ENSP00000343764.6:p.Trp20320Ter
ENST00000342992.11:c.60959G>A (TTN)	ENSP00000343764.6:p.Trp20320Ter
ENST00000359218.10:c.41843G>A (TTN)	ENSP00000352154.5:p.Trp13948Ter
ENST00000359218.9:c.41843G>A (TTN)	ENSP00000352154.5:p.Trp13948Ter
ENST00000460472.6:c.41468G>A (TTN)	ENSP00000434586.1:p.Trp13823Ter
ENST00000591111.5:c.63740G>A (TTN)	ENSP00000465570.1:p.Trp21247Ter
ENST00000615779.4:c.63740G>A (TTN)	ENSP00000483597.1:p.Trp21247Ter
XM_011511729.1:c.67760G>A (TTN)	XP_011510031.1:p.Trp22587Ter
XM_011511730.1:c.41654G>A (TTN)	XP_011510032.1:p.Trp13885Ter
XM_011511731.1:c.41513G>A (TTN)	XP_011510033.1:p.Trp13838Ter
XM_017004819.1:c.67556G>A (TTN)	XP_016860308.1:p.Trp22519Ter
XM_017004820.1:c.62954G>A (TTN)	XP_016860309.1:p.Trp20985Ter
XM_017004821.1:c.62951G>A (TTN)	XP_016860310.1:p.Trp20984Ter
XM_017004822.1:c.59993G>A (TTN)	XP_016860311.1:p.Trp19998Ter
XM_017004823.1:c.41609G>A (TTN)	XP_016860312.1:p.Trp13870Ter
XM_024453094.1:c.63104G>A (TTN)	XP_024308862.1:p.Trp21035Ter
XM_024453095.1:c.63101G>A (TTN)	XP_024308863.1:p.Trp21034Ter
XM_024453096.1:c.62534G>A (TTN)	XP_024308864.1:p.Trp20845Ter
XM_024453097.1:c.59876G>A (TTN)	XP_024308865.1:p.Trp19959Ter
XM_024453098.1:c.59795G>A (TTN)	XP_024308866.1:p.Trp19932Ter
XM_024453099.1:c.41558G>A (TTN)	XP_024308867.1:p.Trp13853Ter
XM_024453100.1:c.31412G>A (TTN)	XP_024308868.1:p.Trp10471Ter