Canonical Allele Identifier: CA349407008

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395229G>T (hg19) ; chr2:g.178530502G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530502G>T , CM000664.2:g.178530502G>T	GRCh38
NC_000002.11:g.179395229G>T , CM000664.1:g.179395229G>T	GRCh37
NC_000002.10:g.179103475G>T	NCBI36
NG_011618.3:g.305301C>A , LRG_391:g.305301C>A
NG_051363.1:g.12676G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98409C>A (TTN)	ENSP00000343764.6:p.Asn32803Lys
ENST00000342175.11:c.79494C>A (TTN)	ENSP00000340554.6:p.Asn26498Lys
ENST00000359218.10:c.79293C>A (TTN)	ENSP00000352154.5:p.Asn26431Lys
ENST00000342175.10:c.79494C>A (TTN)	ENSP00000340554.6:p.Asn26498Lys
ENST00000342992.10:c.98409C>A (TTN)	ENSP00000343764.6:p.Asn32803Lys
ENST00000359218.9:c.79293C>A (TTN)	ENSP00000352154.5:p.Asn26431Lys
ENST00000460472.6:c.78918C>A (TTN)	ENSP00000434586.1:p.Asn26306Lys
ENST00000589042.5:c.106113C>A (TTN) MANE Select	ENSP00000467141.1:p.Asn35371Lys
ENST00000591111.5:c.101190C>A (TTN)	ENSP00000465570.1:p.Asn33730Lys
ENST00000615779.4:c.101190C>A (TTN)	ENSP00000483597.1:p.Asn33730Lys
NM_001256850.1:c.101190C>A (TTN)	NP_001243779.1:p.Asn33730Lys
NM_001267550.2:c.106113C>A (TTN) MANE Select	NP_001254479.2:p.Asn35371Lys
NM_003319.4:c.78918C>A (TTN)	NP_003310.4:p.Asn26306Lys
NM_133378.4:c.98409C>A (TTN)	NP_596869.4:p.Asn32803Lys
NM_133432.3:c.79293C>A (TTN)	NP_597676.3:p.Asn26431Lys
NM_133437.4:c.79494C>A (TTN)	NP_597681.4:p.Asn26498Lys
NR_038271.1:n.446+6866G>T (TTN-AS1)
NR_038272.1:n.220-5230G>T (TTN-AS1)
XM_011511729.1:c.105210C>A (TTN)	XP_011510031.1:p.Asn35070Lys
XM_011511730.1:c.79104C>A (TTN)	XP_011510032.1:p.Asn26368Lys
XM_011511731.1:c.78963C>A (TTN)	XP_011510033.1:p.Asn26321Lys
XM_017004819.1:c.105006C>A (TTN)	XP_016860308.1:p.Asn35002Lys
XM_017004820.1:c.100404C>A (TTN)	XP_016860309.1:p.Asn33468Lys
XM_017004821.1:c.100401C>A (TTN)	XP_016860310.1:p.Asn33467Lys
XM_017004822.1:c.97443C>A (TTN)	XP_016860311.1:p.Asn32481Lys
XM_017004823.1:c.79059C>A (TTN)	XP_016860312.1:p.Asn26353Lys
XM_024453094.1:c.100554C>A (TTN)	XP_024308862.1:p.Asn33518Lys
XM_024453095.1:c.100551C>A (TTN)	XP_024308863.1:p.Asn33517Lys
XM_024453096.1:c.99984C>A (TTN)	XP_024308864.1:p.Asn33328Lys
XM_024453097.1:c.97326C>A (TTN)	XP_024308865.1:p.Asn32442Lys
XM_024453098.1:c.97245C>A (TTN)	XP_024308866.1:p.Asn32415Lys
XM_024453099.1:c.79008C>A (TTN)	XP_024308867.1:p.Asn26336Lys
XM_024453100.1:c.68862C>A (TTN)	XP_024308868.1:p.Asn22954Lys