Canonical Allele Identifier: CA430235952

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396981T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532254T>C , CM000664.2:g.178532254T>C	GRCh38
NC_000002.11:g.179396981T>C , CM000664.1:g.179396981T>C	GRCh37
NC_000002.10:g.179105227T>C	NCBI36
NG_011618.3:g.303549A>G , LRG_391:g.303549A>G
NG_051363.1:g.14428T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96657A>G (TTN)	ENSP00000343764.6:p.Lys32219=
ENST00000342175.11:c.77742A>G (TTN)	ENSP00000340554.6:p.Lys25914=
ENST00000359218.10:c.77541A>G (TTN)	ENSP00000352154.5:p.Lys25847=
ENST00000342175.10:c.77742A>G (TTN)	ENSP00000340554.6:p.Lys25914=
ENST00000342992.10:c.96657A>G (TTN)	ENSP00000343764.6:p.Lys32219=
ENST00000359218.9:c.77541A>G (TTN)	ENSP00000352154.5:p.Lys25847=
ENST00000460472.6:c.77166A>G (TTN)	ENSP00000434586.1:p.Lys25722=
ENST00000589042.5:c.104361A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys34787=
ENST00000591111.5:c.99438A>G (TTN)	ENSP00000465570.1:p.Lys33146=
ENST00000615779.4:c.99438A>G (TTN)	ENSP00000483597.1:p.Lys33146=
NM_001256850.1:c.99438A>G (TTN)	NP_001243779.1:p.Lys33146=
NM_001267550.2:c.104361A>G (TTN) MANE Select	NP_001254479.2:p.Lys34787=
NM_003319.4:c.77166A>G (TTN)	NP_003310.4:p.Lys25722=
NM_133378.4:c.96657A>G (TTN)	NP_596869.4:p.Lys32219=
NM_133432.3:c.77541A>G (TTN)	NP_597676.3:p.Lys25847=
NM_133437.4:c.77742A>G (TTN)	NP_597681.4:p.Lys25914=
NR_038271.1:n.446+8618T>C (TTN-AS1)
NR_038272.1:n.220-3478T>C (TTN-AS1)
XM_011511729.1:c.103458A>G (TTN)	XP_011510031.1:p.Lys34486=
XM_011511730.1:c.77352A>G (TTN)	XP_011510032.1:p.Lys25784=
XM_011511731.1:c.77211A>G (TTN)	XP_011510033.1:p.Lys25737=
XM_017004819.1:c.103254A>G (TTN)	XP_016860308.1:p.Lys34418=
XM_017004820.1:c.98652A>G (TTN)	XP_016860309.1:p.Lys32884=
XM_017004821.1:c.98649A>G (TTN)	XP_016860310.1:p.Lys32883=
XM_017004822.1:c.95691A>G (TTN)	XP_016860311.1:p.Lys31897=
XM_017004823.1:c.77307A>G (TTN)	XP_016860312.1:p.Lys25769=
XM_024453094.1:c.98802A>G (TTN)	XP_024308862.1:p.Lys32934=
XM_024453095.1:c.98799A>G (TTN)	XP_024308863.1:p.Lys32933=
XM_024453096.1:c.98232A>G (TTN)	XP_024308864.1:p.Lys32744=
XM_024453097.1:c.95574A>G (TTN)	XP_024308865.1:p.Lys31858=
XM_024453098.1:c.95493A>G (TTN)	XP_024308866.1:p.Lys31831=
XM_024453099.1:c.77256A>G (TTN)	XP_024308867.1:p.Lys25752=
XM_024453100.1:c.67110A>G (TTN)	XP_024308868.1:p.Lys22370=