Canonical Allele Identifier: CA430113580

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179495059G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630332G>C , CM000664.2:g.178630332G>C	GRCh38
NC_000002.11:g.179495059G>C , CM000664.1:g.179495059G>C	GRCh37
NC_000002.10:g.179203304G>C	NCBI36
NG_011618.3:g.205471C>G , LRG_391:g.205471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.36486C>G	ENSP00000343764.6:p.Ser12162=
ENST00000342175.11:c.17571C>G	ENSP00000340554.6:p.Ser5857=
ENST00000359218.10:c.17370C>G	ENSP00000352154.5:p.Ser5790=
ENST00000342175.10:c.17571C>G	ENSP00000340554.6:p.Ser5857=
ENST00000342992.10:c.36486C>G	ENSP00000343764.6:p.Ser12162=
ENST00000359218.9:c.17370C>G	ENSP00000352154.5:p.Ser5790=
ENST00000460472.6:c.16995C>G	ENSP00000434586.1:p.Ser5665=
ENST00000589042.5:c.44190C>G MANE Select	ENSP00000467141.1:p.Ser14730=
ENST00000591111.5:c.39267C>G	ENSP00000465570.1:p.Ser13089=
ENST00000615779.4:c.39267C>G	ENSP00000483597.1:p.Ser13089=
NM_001256850.1:c.39267C>G	NP_001243779.1:p.Ser13089=
NM_001267550.2:c.44190C>G MANE Select	NP_001254479.2:p.Ser14730=
NM_003319.4:c.16995C>G	NP_003310.4:p.Ser5665=
NM_133378.4:c.36486C>G	NP_596869.4:p.Ser12162=
NM_133432.3:c.17370C>G	NP_597676.3:p.Ser5790=
NM_133437.4:c.17571C>G	NP_597681.4:p.Ser5857=
XM_011511729.1:c.43287C>G	XP_011510031.1:p.Ser14429=
XM_011511730.1:c.17181C>G	XP_011510032.1:p.Ser5727=
XM_011511731.1:c.17040C>G	XP_011510033.1:p.Ser5680=
XM_017004819.1:c.43083C>G	XP_016860308.1:p.Ser14361=
XM_017004820.1:c.38481C>G	XP_016860309.1:p.Ser12827=
XM_017004821.1:c.38478C>G	XP_016860310.1:p.Ser12826=
XM_017004822.1:c.35520C>G	XP_016860311.1:p.Ser11840=
XM_017004823.1:c.17136C>G	XP_016860312.1:p.Ser5712=
XM_024453094.1:c.38631C>G	XP_024308862.1:p.Ser12877=
XM_024453095.1:c.38628C>G	XP_024308863.1:p.Ser12876=
XM_024453096.1:c.38061C>G	XP_024308864.1:p.Ser12687=
XM_024453097.1:c.35403C>G	XP_024308865.1:p.Ser11801=
XM_024453098.1:c.35322C>G	XP_024308866.1:p.Ser11774=
XM_024453099.1:c.17085C>G	XP_024308867.1:p.Ser5695=
XM_024453100.1:c.6939C>G	XP_024308868.1:p.Ser2313=