Canonical Allele Identifier: CA349407227

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395332G>T (hg19) ; chr2:g.178530605G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530605G>T , CM000664.2:g.178530605G>T	GRCh38
NC_000002.11:g.179395332G>T , CM000664.1:g.179395332G>T	GRCh37
NC_000002.10:g.179103578G>T	NCBI36
NG_011618.3:g.305198C>A , LRG_391:g.305198C>A
NG_051363.1:g.12779G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98306C>A (TTN)	ENSP00000343764.6:p.Ser32769Ter
ENST00000342175.11:c.79391C>A (TTN)	ENSP00000340554.6:p.Ser26464Ter
ENST00000359218.10:c.79190C>A (TTN)	ENSP00000352154.5:p.Ser26397Ter
ENST00000342175.10:c.79391C>A (TTN)	ENSP00000340554.6:p.Ser26464Ter
ENST00000342992.10:c.98306C>A (TTN)	ENSP00000343764.6:p.Ser32769Ter
ENST00000359218.9:c.79190C>A (TTN)	ENSP00000352154.5:p.Ser26397Ter
ENST00000460472.6:c.78815C>A (TTN)	ENSP00000434586.1:p.Ser26272Ter
ENST00000589042.5:c.106010C>A (TTN) MANE Select	ENSP00000467141.1:p.Ser35337Ter
ENST00000591111.5:c.101087C>A (TTN)	ENSP00000465570.1:p.Ser33696Ter
ENST00000615779.4:c.101087C>A (TTN)	ENSP00000483597.1:p.Ser33696Ter
NM_001256850.1:c.101087C>A (TTN)	NP_001243779.1:p.Ser33696Ter
NM_001267550.2:c.106010C>A (TTN) MANE Select	NP_001254479.2:p.Ser35337Ter
NM_003319.4:c.78815C>A (TTN)	NP_003310.4:p.Ser26272Ter
NM_133378.4:c.98306C>A (TTN)	NP_596869.4:p.Ser32769Ter
NM_133432.3:c.79190C>A (TTN)	NP_597676.3:p.Ser26397Ter
NM_133437.4:c.79391C>A (TTN)	NP_597681.4:p.Ser26464Ter
NR_038271.1:n.446+6969G>T (TTN-AS1)
NR_038272.1:n.220-5127G>T (TTN-AS1)
XM_011511729.1:c.105107C>A (TTN)	XP_011510031.1:p.Ser35036Ter
XM_011511730.1:c.79001C>A (TTN)	XP_011510032.1:p.Ser26334Ter
XM_011511731.1:c.78860C>A (TTN)	XP_011510033.1:p.Ser26287Ter
XM_017004819.1:c.104903C>A (TTN)	XP_016860308.1:p.Ser34968Ter
XM_017004820.1:c.100301C>A (TTN)	XP_016860309.1:p.Ser33434Ter
XM_017004821.1:c.100298C>A (TTN)	XP_016860310.1:p.Ser33433Ter
XM_017004822.1:c.97340C>A (TTN)	XP_016860311.1:p.Ser32447Ter
XM_017004823.1:c.78956C>A (TTN)	XP_016860312.1:p.Ser26319Ter
XM_024453094.1:c.100451C>A (TTN)	XP_024308862.1:p.Ser33484Ter
XM_024453095.1:c.100448C>A (TTN)	XP_024308863.1:p.Ser33483Ter
XM_024453096.1:c.99881C>A (TTN)	XP_024308864.1:p.Ser33294Ter
XM_024453097.1:c.97223C>A (TTN)	XP_024308865.1:p.Ser32408Ter
XM_024453098.1:c.97142C>A (TTN)	XP_024308866.1:p.Ser32381Ter
XM_024453099.1:c.78905C>A (TTN)	XP_024308867.1:p.Ser26302Ter
XM_024453100.1:c.68759C>A (TTN)	XP_024308868.1:p.Ser22920Ter