Canonical Allele Identifier: CA430113585

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179495065T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630338T>A , CM000664.2:g.178630338T>A	GRCh38
NC_000002.11:g.179495065T>A , CM000664.1:g.179495065T>A	GRCh37
NC_000002.10:g.179203310T>A	NCBI36
NG_011618.3:g.205465A>T , LRG_391:g.205465A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36480A>T	ENSP00000343764.6:p.Ile12160=
ENST00000342175.11:c.17565A>T	ENSP00000340554.6:p.Ile5855=
ENST00000359218.10:c.17364A>T	ENSP00000352154.5:p.Ile5788=
ENST00000342175.10:c.17565A>T	ENSP00000340554.6:p.Ile5855=
ENST00000342992.10:c.36480A>T	ENSP00000343764.6:p.Ile12160=
ENST00000359218.9:c.17364A>T	ENSP00000352154.5:p.Ile5788=
ENST00000460472.6:c.16989A>T	ENSP00000434586.1:p.Ile5663=
ENST00000589042.5:c.44184A>T MANE Select	ENSP00000467141.1:p.Ile14728=
ENST00000591111.5:c.39261A>T	ENSP00000465570.1:p.Ile13087=
ENST00000615779.4:c.39261A>T	ENSP00000483597.1:p.Ile13087=
NM_001256850.1:c.39261A>T	NP_001243779.1:p.Ile13087=
NM_001267550.2:c.44184A>T MANE Select	NP_001254479.2:p.Ile14728=
NM_003319.4:c.16989A>T	NP_003310.4:p.Ile5663=
NM_133378.4:c.36480A>T	NP_596869.4:p.Ile12160=
NM_133432.3:c.17364A>T	NP_597676.3:p.Ile5788=
NM_133437.4:c.17565A>T	NP_597681.4:p.Ile5855=
XM_011511729.1:c.43281A>T	XP_011510031.1:p.Ile14427=
XM_011511730.1:c.17175A>T	XP_011510032.1:p.Ile5725=
XM_011511731.1:c.17034A>T	XP_011510033.1:p.Ile5678=
XM_017004819.1:c.43077A>T	XP_016860308.1:p.Ile14359=
XM_017004820.1:c.38475A>T	XP_016860309.1:p.Ile12825=
XM_017004821.1:c.38472A>T	XP_016860310.1:p.Ile12824=
XM_017004822.1:c.35514A>T	XP_016860311.1:p.Ile11838=
XM_017004823.1:c.17130A>T	XP_016860312.1:p.Ile5710=
XM_024453094.1:c.38625A>T	XP_024308862.1:p.Ile12875=
XM_024453095.1:c.38622A>T	XP_024308863.1:p.Ile12874=
XM_024453096.1:c.38055A>T	XP_024308864.1:p.Ile12685=
XM_024453097.1:c.35397A>T	XP_024308865.1:p.Ile11799=
XM_024453098.1:c.35316A>T	XP_024308866.1:p.Ile11772=
XM_024453099.1:c.17079A>T	XP_024308867.1:p.Ile5693=
XM_024453100.1:c.6933A>T	XP_024308868.1:p.Ile2311=