Canonical Allele Identifier: CA349411961

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96634A>G (TTN)	ENSP00000343764.6:p.Thr32212Ala
ENST00000342175.11:c.77719A>G (TTN)	ENSP00000340554.6:p.Thr25907Ala
ENST00000359218.10:c.77518A>G (TTN)	ENSP00000352154.5:p.Thr25840Ala
ENST00000342175.10:c.77719A>G (TTN)	ENSP00000340554.6:p.Thr25907Ala
ENST00000342992.10:c.96634A>G (TTN)	ENSP00000343764.6:p.Thr32212Ala
ENST00000359218.9:c.77518A>G (TTN)	ENSP00000352154.5:p.Thr25840Ala
ENST00000460472.6:c.77143A>G (TTN)	ENSP00000434586.1:p.Thr25715Ala
ENST00000589042.5:c.104338A>G (TTN) MANE Select	ENSP00000467141.1:p.Thr34780Ala
ENST00000591111.5:c.99415A>G (TTN)	ENSP00000465570.1:p.Thr33139Ala
ENST00000615779.4:c.99415A>G (TTN)	ENSP00000483597.1:p.Thr33139Ala
NM_001256850.1:c.99415A>G (TTN)	NP_001243779.1:p.Thr33139Ala
NM_001267550.2:c.104338A>G (TTN) MANE Select	NP_001254479.2:p.Thr34780Ala
NM_003319.4:c.77143A>G (TTN)	NP_003310.4:p.Thr25715Ala
NM_133378.4:c.96634A>G (TTN)	NP_596869.4:p.Thr32212Ala
NM_133432.3:c.77518A>G (TTN)	NP_597676.3:p.Thr25840Ala
NM_133437.4:c.77719A>G (TTN)	NP_597681.4:p.Thr25907Ala
NR_038271.1:n.446+8641T>C (TTN-AS1)
NR_038272.1:n.220-3455T>C (TTN-AS1)
XM_011511729.1:c.103435A>G (TTN)	XP_011510031.1:p.Thr34479Ala
XM_011511730.1:c.77329A>G (TTN)	XP_011510032.1:p.Thr25777Ala
XM_011511731.1:c.77188A>G (TTN)	XP_011510033.1:p.Thr25730Ala
XM_017004819.1:c.103231A>G (TTN)	XP_016860308.1:p.Thr34411Ala
XM_017004820.1:c.98629A>G (TTN)	XP_016860309.1:p.Thr32877Ala
XM_017004821.1:c.98626A>G (TTN)	XP_016860310.1:p.Thr32876Ala
XM_017004822.1:c.95668A>G (TTN)	XP_016860311.1:p.Thr31890Ala
XM_017004823.1:c.77284A>G (TTN)	XP_016860312.1:p.Thr25762Ala
XM_024453094.1:c.98779A>G (TTN)	XP_024308862.1:p.Thr32927Ala
XM_024453095.1:c.98776A>G (TTN)	XP_024308863.1:p.Thr32926Ala
XM_024453096.1:c.98209A>G (TTN)	XP_024308864.1:p.Thr32737Ala
XM_024453097.1:c.95551A>G (TTN)	XP_024308865.1:p.Thr31851Ala
XM_024453098.1:c.95470A>G (TTN)	XP_024308866.1:p.Thr31824Ala
XM_024453099.1:c.77233A>G (TTN)	XP_024308867.1:p.Thr25745Ala
XM_024453100.1:c.67087A>G (TTN)	XP_024308868.1:p.Thr22363Ala