Canonical Allele Identifier: CA349405516

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394818T>G (hg19) ; chr2:g.178530091T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530091T>G , CM000664.2:g.178530091T>G	GRCh38
NC_000002.11:g.179394818T>G , CM000664.1:g.179394818T>G	GRCh37
NC_000002.10:g.179103064T>G	NCBI36
NG_011618.3:g.305712A>C , LRG_391:g.305712A>C
NG_051363.1:g.12265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98696A>C (TTN)	ENSP00000343764.6:p.Lys32899Thr
ENST00000342175.11:c.79781A>C (TTN)	ENSP00000340554.6:p.Lys26594Thr
ENST00000359218.10:c.79580A>C (TTN)	ENSP00000352154.5:p.Lys26527Thr
ENST00000342175.10:c.79781A>C (TTN)	ENSP00000340554.6:p.Lys26594Thr
ENST00000342992.10:c.98696A>C (TTN)	ENSP00000343764.6:p.Lys32899Thr
ENST00000359218.9:c.79580A>C (TTN)	ENSP00000352154.5:p.Lys26527Thr
ENST00000460472.6:c.79205A>C (TTN)	ENSP00000434586.1:p.Lys26402Thr
ENST00000589042.5:c.106400A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys35467Thr
ENST00000591111.5:c.101477A>C (TTN)	ENSP00000465570.1:p.Lys33826Thr
ENST00000615779.4:c.101477A>C (TTN)	ENSP00000483597.1:p.Lys33826Thr
NM_001256850.1:c.101477A>C (TTN)	NP_001243779.1:p.Lys33826Thr
NM_001267550.2:c.106400A>C (TTN) MANE Select	NP_001254479.2:p.Lys35467Thr
NM_003319.4:c.79205A>C (TTN)	NP_003310.4:p.Lys26402Thr
NM_133378.4:c.98696A>C (TTN)	NP_596869.4:p.Lys32899Thr
NM_133432.3:c.79580A>C (TTN)	NP_597676.3:p.Lys26527Thr
NM_133437.4:c.79781A>C (TTN)	NP_597681.4:p.Lys26594Thr
NR_038271.1:n.446+6455T>G (TTN-AS1)
NR_038272.1:n.220-5641T>G (TTN-AS1)
XM_011511729.1:c.105497A>C (TTN)	XP_011510031.1:p.Lys35166Thr
XM_011511730.1:c.79391A>C (TTN)	XP_011510032.1:p.Lys26464Thr
XM_011511731.1:c.79250A>C (TTN)	XP_011510033.1:p.Lys26417Thr
XM_017004819.1:c.105293A>C (TTN)	XP_016860308.1:p.Lys35098Thr
XM_017004820.1:c.100691A>C (TTN)	XP_016860309.1:p.Lys33564Thr
XM_017004821.1:c.100688A>C (TTN)	XP_016860310.1:p.Lys33563Thr
XM_017004822.1:c.97730A>C (TTN)	XP_016860311.1:p.Lys32577Thr
XM_017004823.1:c.79346A>C (TTN)	XP_016860312.1:p.Lys26449Thr
XM_024453094.1:c.100841A>C (TTN)	XP_024308862.1:p.Lys33614Thr
XM_024453095.1:c.100838A>C (TTN)	XP_024308863.1:p.Lys33613Thr
XM_024453096.1:c.100271A>C (TTN)	XP_024308864.1:p.Lys33424Thr
XM_024453097.1:c.97613A>C (TTN)	XP_024308865.1:p.Lys32538Thr
XM_024453098.1:c.97532A>C (TTN)	XP_024308866.1:p.Lys32511Thr
XM_024453099.1:c.79295A>C (TTN)	XP_024308867.1:p.Lys26432Thr
XM_024453100.1:c.69149A>C (TTN)	XP_024308868.1:p.Lys23050Thr