Canonical Allele Identifier: CA349405622

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394839A>T (hg19) ; chr2:g.178530112A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530112A>T , CM000664.2:g.178530112A>T	GRCh38
NC_000002.11:g.179394839A>T , CM000664.1:g.179394839A>T	GRCh37
NC_000002.10:g.179103085A>T	NCBI36
NG_011618.3:g.305691T>A , LRG_391:g.305691T>A
NG_051363.1:g.12286A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98675T>A (TTN)	ENSP00000343764.6:p.Ile32892Asn
ENST00000342175.11:c.79760T>A (TTN)	ENSP00000340554.6:p.Ile26587Asn
ENST00000359218.10:c.79559T>A (TTN)	ENSP00000352154.5:p.Ile26520Asn
ENST00000342175.10:c.79760T>A (TTN)	ENSP00000340554.6:p.Ile26587Asn
ENST00000342992.10:c.98675T>A (TTN)	ENSP00000343764.6:p.Ile32892Asn
ENST00000359218.9:c.79559T>A (TTN)	ENSP00000352154.5:p.Ile26520Asn
ENST00000460472.6:c.79184T>A (TTN)	ENSP00000434586.1:p.Ile26395Asn
ENST00000589042.5:c.106379T>A (TTN) MANE Select	ENSP00000467141.1:p.Ile35460Asn
ENST00000591111.5:c.101456T>A (TTN)	ENSP00000465570.1:p.Ile33819Asn
ENST00000615779.4:c.101456T>A (TTN)	ENSP00000483597.1:p.Ile33819Asn
NM_001256850.1:c.101456T>A (TTN)	NP_001243779.1:p.Ile33819Asn
NM_001267550.2:c.106379T>A (TTN) MANE Select	NP_001254479.2:p.Ile35460Asn
NM_003319.4:c.79184T>A (TTN)	NP_003310.4:p.Ile26395Asn
NM_133378.4:c.98675T>A (TTN)	NP_596869.4:p.Ile32892Asn
NM_133432.3:c.79559T>A (TTN)	NP_597676.3:p.Ile26520Asn
NM_133437.4:c.79760T>A (TTN)	NP_597681.4:p.Ile26587Asn
NR_038271.1:n.446+6476A>T (TTN-AS1)
NR_038272.1:n.220-5620A>T (TTN-AS1)
XM_011511729.1:c.105476T>A (TTN)	XP_011510031.1:p.Ile35159Asn
XM_011511730.1:c.79370T>A (TTN)	XP_011510032.1:p.Ile26457Asn
XM_011511731.1:c.79229T>A (TTN)	XP_011510033.1:p.Ile26410Asn
XM_017004819.1:c.105272T>A (TTN)	XP_016860308.1:p.Ile35091Asn
XM_017004820.1:c.100670T>A (TTN)	XP_016860309.1:p.Ile33557Asn
XM_017004821.1:c.100667T>A (TTN)	XP_016860310.1:p.Ile33556Asn
XM_017004822.1:c.97709T>A (TTN)	XP_016860311.1:p.Ile32570Asn
XM_017004823.1:c.79325T>A (TTN)	XP_016860312.1:p.Ile26442Asn
XM_024453094.1:c.100820T>A (TTN)	XP_024308862.1:p.Ile33607Asn
XM_024453095.1:c.100817T>A (TTN)	XP_024308863.1:p.Ile33606Asn
XM_024453096.1:c.100250T>A (TTN)	XP_024308864.1:p.Ile33417Asn
XM_024453097.1:c.97592T>A (TTN)	XP_024308865.1:p.Ile32531Asn
XM_024453098.1:c.97511T>A (TTN)	XP_024308866.1:p.Ile32504Asn
XM_024453099.1:c.79274T>A (TTN)	XP_024308867.1:p.Ile26425Asn
XM_024453100.1:c.69128T>A (TTN)	XP_024308868.1:p.Ile23043Asn