Canonical Allele Identifier: CA430271222

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179472408A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607681A>G , CM000664.2:g.178607681A>G	GRCh38
NC_000002.11:g.179472408A>G , CM000664.1:g.179472408A>G	GRCh37
NC_000002.10:g.179180653A>G	NCBI36
NG_011618.3:g.228122T>C , LRG_391:g.228122T>C
NG_051363.1:g.89855A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45303T>C (TTN)	ENSP00000343764.6:p.Pro15101=
ENST00000342175.11:c.26388T>C (TTN)	ENSP00000340554.6:p.Pro8796=
ENST00000359218.10:c.26187T>C (TTN)	ENSP00000352154.5:p.Pro8729=
ENST00000342175.10:c.26388T>C (TTN)	ENSP00000340554.6:p.Pro8796=
ENST00000342992.10:c.45303T>C (TTN)	ENSP00000343764.6:p.Pro15101=
ENST00000359218.9:c.26187T>C (TTN)	ENSP00000352154.5:p.Pro8729=
ENST00000460472.6:c.25812T>C (TTN)	ENSP00000434586.1:p.Pro8604=
ENST00000589042.5:c.53007T>C (TTN) MANE Select	ENSP00000467141.1:p.Pro17669=
ENST00000591111.5:c.48084T>C (TTN)	ENSP00000465570.1:p.Pro16028=
ENST00000615779.4:c.48084T>C (TTN)	ENSP00000483597.1:p.Pro16028=
NM_001256850.1:c.48084T>C (TTN)	NP_001243779.1:p.Pro16028=
NM_001267550.2:c.53007T>C (TTN) MANE Select	NP_001254479.2:p.Pro17669=
NM_003319.4:c.25812T>C (TTN)	NP_003310.4:p.Pro8604=
NM_133378.4:c.45303T>C (TTN)	NP_596869.4:p.Pro15101=
NM_133432.3:c.26187T>C (TTN)	NP_597676.3:p.Pro8729=
NM_133437.4:c.26388T>C (TTN)	NP_597681.4:p.Pro8796=
NR_038271.1:n.683-486A>G (TTN-AS1)
XM_011511729.1:c.52104T>C (TTN)	XP_011510031.1:p.Pro17368=
XM_011511730.1:c.25998T>C (TTN)	XP_011510032.1:p.Pro8666=
XM_011511731.1:c.25857T>C (TTN)	XP_011510033.1:p.Pro8619=
XM_017004819.1:c.51900T>C (TTN)	XP_016860308.1:p.Pro17300=
XM_017004820.1:c.47298T>C (TTN)	XP_016860309.1:p.Pro15766=
XM_017004821.1:c.47295T>C (TTN)	XP_016860310.1:p.Pro15765=
XM_017004822.1:c.44337T>C (TTN)	XP_016860311.1:p.Pro14779=
XM_017004823.1:c.25953T>C (TTN)	XP_016860312.1:p.Pro8651=
XM_024453094.1:c.47448T>C (TTN)	XP_024308862.1:p.Pro15816=
XM_024453095.1:c.47445T>C (TTN)	XP_024308863.1:p.Pro15815=
XM_024453096.1:c.46878T>C (TTN)	XP_024308864.1:p.Pro15626=
XM_024453097.1:c.44220T>C (TTN)	XP_024308865.1:p.Pro14740=
XM_024453098.1:c.44139T>C (TTN)	XP_024308866.1:p.Pro14713=
XM_024453099.1:c.25902T>C (TTN)	XP_024308867.1:p.Pro8634=
XM_024453100.1:c.15756T>C (TTN)	XP_024308868.1:p.Pro5252=