Canonical Allele Identifier: CA430235901

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396882T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532155T>C , CM000664.2:g.178532155T>C	GRCh38
NC_000002.11:g.179396882T>C , CM000664.1:g.179396882T>C	GRCh37
NC_000002.10:g.179105128T>C	NCBI36
NG_011618.3:g.303648A>G , LRG_391:g.303648A>G
NG_051363.1:g.14329T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96756A>G (TTN)	ENSP00000343764.6:p.Glu32252=
ENST00000342175.11:c.77841A>G (TTN)	ENSP00000340554.6:p.Glu25947=
ENST00000359218.10:c.77640A>G (TTN)	ENSP00000352154.5:p.Glu25880=
ENST00000342175.10:c.77841A>G (TTN)	ENSP00000340554.6:p.Glu25947=
ENST00000342992.10:c.96756A>G (TTN)	ENSP00000343764.6:p.Glu32252=
ENST00000359218.9:c.77640A>G (TTN)	ENSP00000352154.5:p.Glu25880=
ENST00000460472.6:c.77265A>G (TTN)	ENSP00000434586.1:p.Glu25755=
ENST00000589042.5:c.104460A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu34820=
ENST00000591111.5:c.99537A>G (TTN)	ENSP00000465570.1:p.Glu33179=
ENST00000615779.4:c.99537A>G (TTN)	ENSP00000483597.1:p.Glu33179=
NM_001256850.1:c.99537A>G (TTN)	NP_001243779.1:p.Glu33179=
NM_001267550.2:c.104460A>G (TTN) MANE Select	NP_001254479.2:p.Glu34820=
NM_003319.4:c.77265A>G (TTN)	NP_003310.4:p.Glu25755=
NM_133378.4:c.96756A>G (TTN)	NP_596869.4:p.Glu32252=
NM_133432.3:c.77640A>G (TTN)	NP_597676.3:p.Glu25880=
NM_133437.4:c.77841A>G (TTN)	NP_597681.4:p.Glu25947=
NR_038271.1:n.446+8519T>C (TTN-AS1)
NR_038272.1:n.220-3577T>C (TTN-AS1)
XM_011511729.1:c.103557A>G (TTN)	XP_011510031.1:p.Glu34519=
XM_011511730.1:c.77451A>G (TTN)	XP_011510032.1:p.Glu25817=
XM_011511731.1:c.77310A>G (TTN)	XP_011510033.1:p.Glu25770=
XM_017004819.1:c.103353A>G (TTN)	XP_016860308.1:p.Glu34451=
XM_017004820.1:c.98751A>G (TTN)	XP_016860309.1:p.Glu32917=
XM_017004821.1:c.98748A>G (TTN)	XP_016860310.1:p.Glu32916=
XM_017004822.1:c.95790A>G (TTN)	XP_016860311.1:p.Glu31930=
XM_017004823.1:c.77406A>G (TTN)	XP_016860312.1:p.Glu25802=
XM_024453094.1:c.98901A>G (TTN)	XP_024308862.1:p.Glu32967=
XM_024453095.1:c.98898A>G (TTN)	XP_024308863.1:p.Glu32966=
XM_024453096.1:c.98331A>G (TTN)	XP_024308864.1:p.Glu32777=
XM_024453097.1:c.95673A>G (TTN)	XP_024308865.1:p.Glu31891=
XM_024453098.1:c.95592A>G (TTN)	XP_024308866.1:p.Glu31864=
XM_024453099.1:c.77355A>G (TTN)	XP_024308867.1:p.Glu25785=
XM_024453100.1:c.67209A>G (TTN)	XP_024308868.1:p.Glu22403=