Canonical Allele Identifier: CA349456771

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409102C>T (hg19) ; chr2:g.178544375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544375C>T , CM000664.2:g.178544375C>T	GRCh38
NC_000002.11:g.179409102C>T , CM000664.1:g.179409102C>T	GRCh37
NC_000002.10:g.179117348C>T	NCBI36
NG_011618.3:g.291428G>A , LRG_391:g.291428G>A
NG_051363.1:g.26549C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.88150G>A (TTN)	ENSP00000343764.6:p.Asp29384Asn
ENST00000342175.11:c.69235G>A (TTN)	ENSP00000340554.6:p.Asp23079Asn
ENST00000359218.10:c.69034G>A (TTN)	ENSP00000352154.5:p.Asp23012Asn
ENST00000342175.10:c.69235G>A (TTN)	ENSP00000340554.6:p.Asp23079Asn
ENST00000342992.10:c.88150G>A (TTN)	ENSP00000343764.6:p.Asp29384Asn
ENST00000359218.9:c.69034G>A (TTN)	ENSP00000352154.5:p.Asp23012Asn
ENST00000460472.6:c.68659G>A (TTN)	ENSP00000434586.1:p.Asp22887Asn
ENST00000589042.5:c.95854G>A (TTN) MANE Select	ENSP00000467141.1:p.Asp31952Asn
ENST00000591111.5:c.90931G>A (TTN)	ENSP00000465570.1:p.Asp30311Asn
ENST00000615779.4:c.90931G>A (TTN)	ENSP00000483597.1:p.Asp30311Asn
NM_001256850.1:c.90931G>A (TTN)	NP_001243779.1:p.Asp30311Asn
NM_001267550.2:c.95854G>A (TTN) MANE Select	NP_001254479.2:p.Asp31952Asn
NM_003319.4:c.68659G>A (TTN)	NP_003310.4:p.Asp22887Asn
NM_133378.4:c.88150G>A (TTN)	NP_596869.4:p.Asp29384Asn
NM_133432.3:c.69034G>A (TTN)	NP_597676.3:p.Asp23012Asn
NM_133437.4:c.69235G>A (TTN)	NP_597681.4:p.Asp23079Asn
NR_038271.1:n.446+20739C>T (TTN-AS1)
NR_038272.1:n.2043+2014C>T (TTN-AS1)
XM_011511729.1:c.94951G>A (TTN)	XP_011510031.1:p.Asp31651Asn
XM_011511730.1:c.68845G>A (TTN)	XP_011510032.1:p.Asp22949Asn
XM_011511731.1:c.68704G>A (TTN)	XP_011510033.1:p.Asp22902Asn
XM_017004819.1:c.94747G>A (TTN)	XP_016860308.1:p.Asp31583Asn
XM_017004820.1:c.90145G>A (TTN)	XP_016860309.1:p.Asp30049Asn
XM_017004821.1:c.90142G>A (TTN)	XP_016860310.1:p.Asp30048Asn
XM_017004822.1:c.87184G>A (TTN)	XP_016860311.1:p.Asp29062Asn
XM_017004823.1:c.68800G>A (TTN)	XP_016860312.1:p.Asp22934Asn
XM_024453094.1:c.90295G>A (TTN)	XP_024308862.1:p.Asp30099Asn
XM_024453095.1:c.90292G>A (TTN)	XP_024308863.1:p.Asp30098Asn
XM_024453096.1:c.89725G>A (TTN)	XP_024308864.1:p.Asp29909Asn
XM_024453097.1:c.87067G>A (TTN)	XP_024308865.1:p.Asp29023Asn
XM_024453098.1:c.86986G>A (TTN)	XP_024308866.1:p.Asp28996Asn
XM_024453099.1:c.68749G>A (TTN)	XP_024308867.1:p.Asp22917Asn
XM_024453100.1:c.58603G>A (TTN)	XP_024308868.1:p.Asp19535Asn