Canonical Allele Identifier: CA430235957

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396990T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532263T>G , CM000664.2:g.178532263T>G	GRCh38
NC_000002.11:g.179396990T>G , CM000664.1:g.179396990T>G	GRCh37
NC_000002.10:g.179105236T>G	NCBI36
NG_011618.3:g.303540A>C , LRG_391:g.303540A>C
NG_051363.1:g.14437T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96648A>C (TTN)	ENSP00000343764.6:p.Ser32216=
ENST00000342175.11:c.77733A>C (TTN)	ENSP00000340554.6:p.Ser25911=
ENST00000359218.10:c.77532A>C (TTN)	ENSP00000352154.5:p.Ser25844=
ENST00000342175.10:c.77733A>C (TTN)	ENSP00000340554.6:p.Ser25911=
ENST00000342992.10:c.96648A>C (TTN)	ENSP00000343764.6:p.Ser32216=
ENST00000359218.9:c.77532A>C (TTN)	ENSP00000352154.5:p.Ser25844=
ENST00000460472.6:c.77157A>C (TTN)	ENSP00000434586.1:p.Ser25719=
ENST00000589042.5:c.104352A>C (TTN) MANE Select	ENSP00000467141.1:p.Ser34784=
ENST00000591111.5:c.99429A>C (TTN)	ENSP00000465570.1:p.Ser33143=
ENST00000615779.4:c.99429A>C (TTN)	ENSP00000483597.1:p.Ser33143=
NM_001256850.1:c.99429A>C (TTN)	NP_001243779.1:p.Ser33143=
NM_001267550.2:c.104352A>C (TTN) MANE Select	NP_001254479.2:p.Ser34784=
NM_003319.4:c.77157A>C (TTN)	NP_003310.4:p.Ser25719=
NM_133378.4:c.96648A>C (TTN)	NP_596869.4:p.Ser32216=
NM_133432.3:c.77532A>C (TTN)	NP_597676.3:p.Ser25844=
NM_133437.4:c.77733A>C (TTN)	NP_597681.4:p.Ser25911=
NR_038271.1:n.446+8627T>G (TTN-AS1)
NR_038272.1:n.220-3469T>G (TTN-AS1)
XM_011511729.1:c.103449A>C (TTN)	XP_011510031.1:p.Ser34483=
XM_011511730.1:c.77343A>C (TTN)	XP_011510032.1:p.Ser25781=
XM_011511731.1:c.77202A>C (TTN)	XP_011510033.1:p.Ser25734=
XM_017004819.1:c.103245A>C (TTN)	XP_016860308.1:p.Ser34415=
XM_017004820.1:c.98643A>C (TTN)	XP_016860309.1:p.Ser32881=
XM_017004821.1:c.98640A>C (TTN)	XP_016860310.1:p.Ser32880=
XM_017004822.1:c.95682A>C (TTN)	XP_016860311.1:p.Ser31894=
XM_017004823.1:c.77298A>C (TTN)	XP_016860312.1:p.Ser25766=
XM_024453094.1:c.98793A>C (TTN)	XP_024308862.1:p.Ser32931=
XM_024453095.1:c.98790A>C (TTN)	XP_024308863.1:p.Ser32930=
XM_024453096.1:c.98223A>C (TTN)	XP_024308864.1:p.Ser32741=
XM_024453097.1:c.95565A>C (TTN)	XP_024308865.1:p.Ser31855=
XM_024453098.1:c.95484A>C (TTN)	XP_024308866.1:p.Ser31828=
XM_024453099.1:c.77247A>C (TTN)	XP_024308867.1:p.Ser25749=
XM_024453100.1:c.67101A>C (TTN)	XP_024308868.1:p.Ser22367=