Canonical Allele Identifier: CA349405627

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394840T>A (hg19) ; chr2:g.178530113T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530113T>A , CM000664.2:g.178530113T>A	GRCh38
NC_000002.11:g.179394840T>A , CM000664.1:g.179394840T>A	GRCh37
NC_000002.10:g.179103086T>A	NCBI36
NG_011618.3:g.305690A>T , LRG_391:g.305690A>T
NG_051363.1:g.12287T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98674A>T (TTN)	ENSP00000343764.6:p.Ile32892Phe
ENST00000342175.11:c.79759A>T (TTN)	ENSP00000340554.6:p.Ile26587Phe
ENST00000359218.10:c.79558A>T (TTN)	ENSP00000352154.5:p.Ile26520Phe
ENST00000342175.10:c.79759A>T (TTN)	ENSP00000340554.6:p.Ile26587Phe
ENST00000342992.10:c.98674A>T (TTN)	ENSP00000343764.6:p.Ile32892Phe
ENST00000359218.9:c.79558A>T (TTN)	ENSP00000352154.5:p.Ile26520Phe
ENST00000460472.6:c.79183A>T (TTN)	ENSP00000434586.1:p.Ile26395Phe
ENST00000589042.5:c.106378A>T (TTN) MANE Select	ENSP00000467141.1:p.Ile35460Phe
ENST00000591111.5:c.101455A>T (TTN)	ENSP00000465570.1:p.Ile33819Phe
ENST00000615779.4:c.101455A>T (TTN)	ENSP00000483597.1:p.Ile33819Phe
NM_001256850.1:c.101455A>T (TTN)	NP_001243779.1:p.Ile33819Phe
NM_001267550.2:c.106378A>T (TTN) MANE Select	NP_001254479.2:p.Ile35460Phe
NM_003319.4:c.79183A>T (TTN)	NP_003310.4:p.Ile26395Phe
NM_133378.4:c.98674A>T (TTN)	NP_596869.4:p.Ile32892Phe
NM_133432.3:c.79558A>T (TTN)	NP_597676.3:p.Ile26520Phe
NM_133437.4:c.79759A>T (TTN)	NP_597681.4:p.Ile26587Phe
NR_038271.1:n.446+6477T>A (TTN-AS1)
NR_038272.1:n.220-5619T>A (TTN-AS1)
XM_011511729.1:c.105475A>T (TTN)	XP_011510031.1:p.Ile35159Phe
XM_011511730.1:c.79369A>T (TTN)	XP_011510032.1:p.Ile26457Phe
XM_011511731.1:c.79228A>T (TTN)	XP_011510033.1:p.Ile26410Phe
XM_017004819.1:c.105271A>T (TTN)	XP_016860308.1:p.Ile35091Phe
XM_017004820.1:c.100669A>T (TTN)	XP_016860309.1:p.Ile33557Phe
XM_017004821.1:c.100666A>T (TTN)	XP_016860310.1:p.Ile33556Phe
XM_017004822.1:c.97708A>T (TTN)	XP_016860311.1:p.Ile32570Phe
XM_017004823.1:c.79324A>T (TTN)	XP_016860312.1:p.Ile26442Phe
XM_024453094.1:c.100819A>T (TTN)	XP_024308862.1:p.Ile33607Phe
XM_024453095.1:c.100816A>T (TTN)	XP_024308863.1:p.Ile33606Phe
XM_024453096.1:c.100249A>T (TTN)	XP_024308864.1:p.Ile33417Phe
XM_024453097.1:c.97591A>T (TTN)	XP_024308865.1:p.Ile32531Phe
XM_024453098.1:c.97510A>T (TTN)	XP_024308866.1:p.Ile32504Phe
XM_024453099.1:c.79273A>T (TTN)	XP_024308867.1:p.Ile26425Phe
XM_024453100.1:c.69127A>T (TTN)	XP_024308868.1:p.Ile23043Phe