Canonical Allele Identifier: CA349411803

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396937T>G (hg19) ; chr2:g.178532210T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532210T>G , CM000664.2:g.178532210T>G	GRCh38
NC_000002.11:g.179396937T>G , CM000664.1:g.179396937T>G	GRCh37
NC_000002.10:g.179105183T>G	NCBI36
NG_011618.3:g.303593A>C , LRG_391:g.303593A>C
NG_051363.1:g.14384T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96701A>C (TTN)	ENSP00000343764.6:p.Lys32234Thr
ENST00000342175.11:c.77786A>C (TTN)	ENSP00000340554.6:p.Lys25929Thr
ENST00000359218.10:c.77585A>C (TTN)	ENSP00000352154.5:p.Lys25862Thr
ENST00000342175.10:c.77786A>C (TTN)	ENSP00000340554.6:p.Lys25929Thr
ENST00000342992.10:c.96701A>C (TTN)	ENSP00000343764.6:p.Lys32234Thr
ENST00000359218.9:c.77585A>C (TTN)	ENSP00000352154.5:p.Lys25862Thr
ENST00000460472.6:c.77210A>C (TTN)	ENSP00000434586.1:p.Lys25737Thr
ENST00000589042.5:c.104405A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys34802Thr
ENST00000591111.5:c.99482A>C (TTN)	ENSP00000465570.1:p.Lys33161Thr
ENST00000615779.4:c.99482A>C (TTN)	ENSP00000483597.1:p.Lys33161Thr
NM_001256850.1:c.99482A>C (TTN)	NP_001243779.1:p.Lys33161Thr
NM_001267550.2:c.104405A>C (TTN) MANE Select	NP_001254479.2:p.Lys34802Thr
NM_003319.4:c.77210A>C (TTN)	NP_003310.4:p.Lys25737Thr
NM_133378.4:c.96701A>C (TTN)	NP_596869.4:p.Lys32234Thr
NM_133432.3:c.77585A>C (TTN)	NP_597676.3:p.Lys25862Thr
NM_133437.4:c.77786A>C (TTN)	NP_597681.4:p.Lys25929Thr
NR_038271.1:n.446+8574T>G (TTN-AS1)
NR_038272.1:n.220-3522T>G (TTN-AS1)
XM_011511729.1:c.103502A>C (TTN)	XP_011510031.1:p.Lys34501Thr
XM_011511730.1:c.77396A>C (TTN)	XP_011510032.1:p.Lys25799Thr
XM_011511731.1:c.77255A>C (TTN)	XP_011510033.1:p.Lys25752Thr
XM_017004819.1:c.103298A>C (TTN)	XP_016860308.1:p.Lys34433Thr
XM_017004820.1:c.98696A>C (TTN)	XP_016860309.1:p.Lys32899Thr
XM_017004821.1:c.98693A>C (TTN)	XP_016860310.1:p.Lys32898Thr
XM_017004822.1:c.95735A>C (TTN)	XP_016860311.1:p.Lys31912Thr
XM_017004823.1:c.77351A>C (TTN)	XP_016860312.1:p.Lys25784Thr
XM_024453094.1:c.98846A>C (TTN)	XP_024308862.1:p.Lys32949Thr
XM_024453095.1:c.98843A>C (TTN)	XP_024308863.1:p.Lys32948Thr
XM_024453096.1:c.98276A>C (TTN)	XP_024308864.1:p.Lys32759Thr
XM_024453097.1:c.95618A>C (TTN)	XP_024308865.1:p.Lys31873Thr
XM_024453098.1:c.95537A>C (TTN)	XP_024308866.1:p.Lys31846Thr
XM_024453099.1:c.77300A>C (TTN)	XP_024308867.1:p.Lys25767Thr
XM_024453100.1:c.67154A>C (TTN)	XP_024308868.1:p.Lys22385Thr