Canonical Allele Identifier: CA349406156

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395028T>G (hg19) ; chr2:g.178530301T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530301T>G , CM000664.2:g.178530301T>G	GRCh38
NC_000002.11:g.179395028T>G , CM000664.1:g.179395028T>G	GRCh37
NC_000002.10:g.179103274T>G	NCBI36
NG_011618.3:g.305502A>C , LRG_391:g.305502A>C
NG_051363.1:g.12475T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98610A>C (TTN)	ENSP00000343764.6:p.Lys32870Asn
ENST00000342175.11:c.79695A>C (TTN)	ENSP00000340554.6:p.Lys26565Asn
ENST00000359218.10:c.79494A>C (TTN)	ENSP00000352154.5:p.Lys26498Asn
ENST00000342175.10:c.79695A>C (TTN)	ENSP00000340554.6:p.Lys26565Asn
ENST00000342992.10:c.98610A>C (TTN)	ENSP00000343764.6:p.Lys32870Asn
ENST00000359218.9:c.79494A>C (TTN)	ENSP00000352154.5:p.Lys26498Asn
ENST00000460472.6:c.79119A>C (TTN)	ENSP00000434586.1:p.Lys26373Asn
ENST00000589042.5:c.106314A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys35438Asn
ENST00000591111.5:c.101391A>C (TTN)	ENSP00000465570.1:p.Lys33797Asn
ENST00000615779.4:c.101391A>C (TTN)	ENSP00000483597.1:p.Lys33797Asn
NM_001256850.1:c.101391A>C (TTN)	NP_001243779.1:p.Lys33797Asn
NM_001267550.2:c.106314A>C (TTN) MANE Select	NP_001254479.2:p.Lys35438Asn
NM_003319.4:c.79119A>C (TTN)	NP_003310.4:p.Lys26373Asn
NM_133378.4:c.98610A>C (TTN)	NP_596869.4:p.Lys32870Asn
NM_133432.3:c.79494A>C (TTN)	NP_597676.3:p.Lys26498Asn
NM_133437.4:c.79695A>C (TTN)	NP_597681.4:p.Lys26565Asn
NR_038271.1:n.446+6665T>G (TTN-AS1)
NR_038272.1:n.220-5431T>G (TTN-AS1)
XM_011511729.1:c.105411A>C (TTN)	XP_011510031.1:p.Lys35137Asn
XM_011511730.1:c.79305A>C (TTN)	XP_011510032.1:p.Lys26435Asn
XM_011511731.1:c.79164A>C (TTN)	XP_011510033.1:p.Lys26388Asn
XM_017004819.1:c.105207A>C (TTN)	XP_016860308.1:p.Lys35069Asn
XM_017004820.1:c.100605A>C (TTN)	XP_016860309.1:p.Lys33535Asn
XM_017004821.1:c.100602A>C (TTN)	XP_016860310.1:p.Lys33534Asn
XM_017004822.1:c.97644A>C (TTN)	XP_016860311.1:p.Lys32548Asn
XM_017004823.1:c.79260A>C (TTN)	XP_016860312.1:p.Lys26420Asn
XM_024453094.1:c.100755A>C (TTN)	XP_024308862.1:p.Lys33585Asn
XM_024453095.1:c.100752A>C (TTN)	XP_024308863.1:p.Lys33584Asn
XM_024453096.1:c.100185A>C (TTN)	XP_024308864.1:p.Lys33395Asn
XM_024453097.1:c.97527A>C (TTN)	XP_024308865.1:p.Lys32509Asn
XM_024453098.1:c.97446A>C (TTN)	XP_024308866.1:p.Lys32482Asn
XM_024453099.1:c.79209A>C (TTN)	XP_024308867.1:p.Lys26403Asn
XM_024453100.1:c.69063A>C (TTN)	XP_024308868.1:p.Lys23021Asn