Canonical Allele Identifier: CA349411960

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179397004T>G (hg19) ; chr2:g.178532277T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532277T>G , CM000664.2:g.178532277T>G	GRCh38
NC_000002.11:g.179397004T>G , CM000664.1:g.179397004T>G	GRCh37
NC_000002.10:g.179105250T>G	NCBI36
NG_011618.3:g.303526A>C , LRG_391:g.303526A>C
NG_051363.1:g.14451T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96634A>C (TTN)	ENSP00000343764.6:p.Thr32212Pro
ENST00000342175.11:c.77719A>C (TTN)	ENSP00000340554.6:p.Thr25907Pro
ENST00000359218.10:c.77518A>C (TTN)	ENSP00000352154.5:p.Thr25840Pro
ENST00000342175.10:c.77719A>C (TTN)	ENSP00000340554.6:p.Thr25907Pro
ENST00000342992.10:c.96634A>C (TTN)	ENSP00000343764.6:p.Thr32212Pro
ENST00000359218.9:c.77518A>C (TTN)	ENSP00000352154.5:p.Thr25840Pro
ENST00000460472.6:c.77143A>C (TTN)	ENSP00000434586.1:p.Thr25715Pro
ENST00000589042.5:c.104338A>C (TTN) MANE Select	ENSP00000467141.1:p.Thr34780Pro
ENST00000591111.5:c.99415A>C (TTN)	ENSP00000465570.1:p.Thr33139Pro
ENST00000615779.4:c.99415A>C (TTN)	ENSP00000483597.1:p.Thr33139Pro
NM_001256850.1:c.99415A>C (TTN)	NP_001243779.1:p.Thr33139Pro
NM_001267550.2:c.104338A>C (TTN) MANE Select	NP_001254479.2:p.Thr34780Pro
NM_003319.4:c.77143A>C (TTN)	NP_003310.4:p.Thr25715Pro
NM_133378.4:c.96634A>C (TTN)	NP_596869.4:p.Thr32212Pro
NM_133432.3:c.77518A>C (TTN)	NP_597676.3:p.Thr25840Pro
NM_133437.4:c.77719A>C (TTN)	NP_597681.4:p.Thr25907Pro
NR_038271.1:n.446+8641T>G (TTN-AS1)
NR_038272.1:n.220-3455T>G (TTN-AS1)
XM_011511729.1:c.103435A>C (TTN)	XP_011510031.1:p.Thr34479Pro
XM_011511730.1:c.77329A>C (TTN)	XP_011510032.1:p.Thr25777Pro
XM_011511731.1:c.77188A>C (TTN)	XP_011510033.1:p.Thr25730Pro
XM_017004819.1:c.103231A>C (TTN)	XP_016860308.1:p.Thr34411Pro
XM_017004820.1:c.98629A>C (TTN)	XP_016860309.1:p.Thr32877Pro
XM_017004821.1:c.98626A>C (TTN)	XP_016860310.1:p.Thr32876Pro
XM_017004822.1:c.95668A>C (TTN)	XP_016860311.1:p.Thr31890Pro
XM_017004823.1:c.77284A>C (TTN)	XP_016860312.1:p.Thr25762Pro
XM_024453094.1:c.98779A>C (TTN)	XP_024308862.1:p.Thr32927Pro
XM_024453095.1:c.98776A>C (TTN)	XP_024308863.1:p.Thr32926Pro
XM_024453096.1:c.98209A>C (TTN)	XP_024308864.1:p.Thr32737Pro
XM_024453097.1:c.95551A>C (TTN)	XP_024308865.1:p.Thr31851Pro
XM_024453098.1:c.95470A>C (TTN)	XP_024308866.1:p.Thr31824Pro
XM_024453099.1:c.77233A>C (TTN)	XP_024308867.1:p.Thr25745Pro
XM_024453100.1:c.67087A>C (TTN)	XP_024308868.1:p.Thr22363Pro