Canonical Allele Identifier: CA349618609

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482919A>T (hg19) ; chr2:g.178618192A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618192A>T , CM000664.2:g.178618192A>T	GRCh38
NC_000002.11:g.179482919A>T , CM000664.1:g.179482919A>T	GRCh37
NC_000002.10:g.179191164A>T	NCBI36
NG_011618.3:g.217611T>A , LRG_391:g.217611T>A
NG_051363.1:g.100366A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.39562T>A (TTN)	ENSP00000343764.6:p.Tyr13188Asn
ENST00000342175.11:c.20647T>A (TTN)	ENSP00000340554.6:p.Tyr6883Asn
ENST00000359218.10:c.20446T>A (TTN)	ENSP00000352154.5:p.Tyr6816Asn
ENST00000342175.10:c.20647T>A (TTN)	ENSP00000340554.6:p.Tyr6883Asn
ENST00000342992.10:c.39562T>A (TTN)	ENSP00000343764.6:p.Tyr13188Asn
ENST00000359218.9:c.20446T>A (TTN)	ENSP00000352154.5:p.Tyr6816Asn
ENST00000460472.6:c.20071T>A (TTN)	ENSP00000434586.1:p.Tyr6691Asn
ENST00000589042.5:c.47266T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr15756Asn
ENST00000591111.5:c.42343T>A (TTN)	ENSP00000465570.1:p.Tyr14115Asn
ENST00000615779.4:c.42343T>A (TTN)	ENSP00000483597.1:p.Tyr14115Asn
NM_001256850.1:c.42343T>A (TTN)	NP_001243779.1:p.Tyr14115Asn
NM_001267550.2:c.47266T>A (TTN) MANE Select	NP_001254479.2:p.Tyr15756Asn
NM_003319.4:c.20071T>A (TTN)	NP_003310.4:p.Tyr6691Asn
NM_133378.4:c.39562T>A (TTN)	NP_596869.4:p.Tyr13188Asn
NM_133432.3:c.20446T>A (TTN)	NP_597676.3:p.Tyr6816Asn
NM_133437.4:c.20647T>A (TTN)	NP_597681.4:p.Tyr6883Asn
NR_038271.1:n.1605-1561A>T (TTN-AS1)
XM_011511729.1:c.46363T>A (TTN)	XP_011510031.1:p.Tyr15455Asn
XM_011511730.1:c.20257T>A (TTN)	XP_011510032.1:p.Tyr6753Asn
XM_011511731.1:c.20116T>A (TTN)	XP_011510033.1:p.Tyr6706Asn
XM_017004819.1:c.46159T>A (TTN)	XP_016860308.1:p.Tyr15387Asn
XM_017004820.1:c.41557T>A (TTN)	XP_016860309.1:p.Tyr13853Asn
XM_017004821.1:c.41554T>A (TTN)	XP_016860310.1:p.Tyr13852Asn
XM_017004822.1:c.38596T>A (TTN)	XP_016860311.1:p.Tyr12866Asn
XM_017004823.1:c.20212T>A (TTN)	XP_016860312.1:p.Tyr6738Asn
XM_024453094.1:c.41707T>A (TTN)	XP_024308862.1:p.Tyr13903Asn
XM_024453095.1:c.41704T>A (TTN)	XP_024308863.1:p.Tyr13902Asn
XM_024453096.1:c.41137T>A (TTN)	XP_024308864.1:p.Tyr13713Asn
XM_024453097.1:c.38479T>A (TTN)	XP_024308865.1:p.Tyr12827Asn
XM_024453098.1:c.38398T>A (TTN)	XP_024308866.1:p.Tyr12800Asn
XM_024453099.1:c.20161T>A (TTN)	XP_024308867.1:p.Tyr6721Asn
XM_024453100.1:c.10015T>A (TTN)	XP_024308868.1:p.Tyr3339Asn