Canonical Allele Identifier: CA349406265

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395045A>T (hg19) ; chr2:g.178530318A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530318A>T , CM000664.2:g.178530318A>T	GRCh38
NC_000002.11:g.179395045A>T , CM000664.1:g.179395045A>T	GRCh37
NC_000002.10:g.179103291A>T	NCBI36
NG_011618.3:g.305485T>A , LRG_391:g.305485T>A
NG_051363.1:g.12492A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98593T>A (TTN)	ENSP00000343764.6:p.Ser32865Thr
ENST00000342175.11:c.79678T>A (TTN)	ENSP00000340554.6:p.Ser26560Thr
ENST00000359218.10:c.79477T>A (TTN)	ENSP00000352154.5:p.Ser26493Thr
ENST00000342175.10:c.79678T>A (TTN)	ENSP00000340554.6:p.Ser26560Thr
ENST00000342992.10:c.98593T>A (TTN)	ENSP00000343764.6:p.Ser32865Thr
ENST00000359218.9:c.79477T>A (TTN)	ENSP00000352154.5:p.Ser26493Thr
ENST00000460472.6:c.79102T>A (TTN)	ENSP00000434586.1:p.Ser26368Thr
ENST00000589042.5:c.106297T>A (TTN) MANE Select	ENSP00000467141.1:p.Ser35433Thr
ENST00000591111.5:c.101374T>A (TTN)	ENSP00000465570.1:p.Ser33792Thr
ENST00000615779.4:c.101374T>A (TTN)	ENSP00000483597.1:p.Ser33792Thr
NM_001256850.1:c.101374T>A (TTN)	NP_001243779.1:p.Ser33792Thr
NM_001267550.2:c.106297T>A (TTN) MANE Select	NP_001254479.2:p.Ser35433Thr
NM_003319.4:c.79102T>A (TTN)	NP_003310.4:p.Ser26368Thr
NM_133378.4:c.98593T>A (TTN)	NP_596869.4:p.Ser32865Thr
NM_133432.3:c.79477T>A (TTN)	NP_597676.3:p.Ser26493Thr
NM_133437.4:c.79678T>A (TTN)	NP_597681.4:p.Ser26560Thr
NR_038271.1:n.446+6682A>T (TTN-AS1)
NR_038272.1:n.220-5414A>T (TTN-AS1)
XM_011511729.1:c.105394T>A (TTN)	XP_011510031.1:p.Ser35132Thr
XM_011511730.1:c.79288T>A (TTN)	XP_011510032.1:p.Ser26430Thr
XM_011511731.1:c.79147T>A (TTN)	XP_011510033.1:p.Ser26383Thr
XM_017004819.1:c.105190T>A (TTN)	XP_016860308.1:p.Ser35064Thr
XM_017004820.1:c.100588T>A (TTN)	XP_016860309.1:p.Ser33530Thr
XM_017004821.1:c.100585T>A (TTN)	XP_016860310.1:p.Ser33529Thr
XM_017004822.1:c.97627T>A (TTN)	XP_016860311.1:p.Ser32543Thr
XM_017004823.1:c.79243T>A (TTN)	XP_016860312.1:p.Ser26415Thr
XM_024453094.1:c.100738T>A (TTN)	XP_024308862.1:p.Ser33580Thr
XM_024453095.1:c.100735T>A (TTN)	XP_024308863.1:p.Ser33579Thr
XM_024453096.1:c.100168T>A (TTN)	XP_024308864.1:p.Ser33390Thr
XM_024453097.1:c.97510T>A (TTN)	XP_024308865.1:p.Ser32504Thr
XM_024453098.1:c.97429T>A (TTN)	XP_024308866.1:p.Ser32477Thr
XM_024453099.1:c.79192T>A (TTN)	XP_024308867.1:p.Ser26398Thr
XM_024453100.1:c.69046T>A (TTN)	XP_024308868.1:p.Ser23016Thr