Canonical Allele Identifier: CA349658695

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179439620A>C (hg19) ; chr2:g.178574893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178574893A>C , CM000664.2:g.178574893A>C	GRCh38
NC_000002.11:g.179439620A>C , CM000664.1:g.179439620A>C	GRCh37
NC_000002.10:g.179147866A>C	NCBI36
NG_011618.3:g.260910T>G , LRG_391:g.260910T>G
NG_051363.1:g.57067A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.63535T>G (TTN)	ENSP00000343764.6:p.Ser21179Ala
ENST00000342175.11:c.44620T>G (TTN)	ENSP00000340554.6:p.Ser14874Ala
ENST00000359218.10:c.44419T>G (TTN)	ENSP00000352154.5:p.Ser14807Ala
ENST00000342175.10:c.44620T>G (TTN)	ENSP00000340554.6:p.Ser14874Ala
ENST00000342992.10:c.63535T>G (TTN)	ENSP00000343764.6:p.Ser21179Ala
ENST00000359218.9:c.44419T>G (TTN)	ENSP00000352154.5:p.Ser14807Ala
ENST00000460472.6:c.44044T>G (TTN)	ENSP00000434586.1:p.Ser14682Ala
ENST00000589042.5:c.71239T>G (TTN) MANE Select	ENSP00000467141.1:p.Ser23747Ala
ENST00000591111.5:c.66316T>G (TTN)	ENSP00000465570.1:p.Ser22106Ala
ENST00000615779.4:c.66316T>G (TTN)	ENSP00000483597.1:p.Ser22106Ala
NM_001256850.1:c.66316T>G (TTN)	NP_001243779.1:p.Ser22106Ala
NM_001267550.2:c.71239T>G (TTN) MANE Select	NP_001254479.2:p.Ser23747Ala
NM_003319.4:c.44044T>G (TTN)	NP_003310.4:p.Ser14682Ala
NM_133378.4:c.63535T>G (TTN)	NP_596869.4:p.Ser21179Ala
NM_133432.3:c.44419T>G (TTN)	NP_597676.3:p.Ser14807Ala
NM_133437.4:c.44620T>G (TTN)	NP_597681.4:p.Ser14874Ala
NR_038271.1:n.596+3444A>C (TTN-AS1)
NR_038272.1:n.2044-7679A>C (TTN-AS1)
XM_011511729.1:c.70336T>G (TTN)	XP_011510031.1:p.Ser23446Ala
XM_011511730.1:c.44230T>G (TTN)	XP_011510032.1:p.Ser14744Ala
XM_011511731.1:c.44089T>G (TTN)	XP_011510033.1:p.Ser14697Ala
XM_017004819.1:c.70132T>G (TTN)	XP_016860308.1:p.Ser23378Ala
XM_017004820.1:c.65530T>G (TTN)	XP_016860309.1:p.Ser21844Ala
XM_017004821.1:c.65527T>G (TTN)	XP_016860310.1:p.Ser21843Ala
XM_017004822.1:c.62569T>G (TTN)	XP_016860311.1:p.Ser20857Ala
XM_017004823.1:c.44185T>G (TTN)	XP_016860312.1:p.Ser14729Ala
XM_024453094.1:c.65680T>G (TTN)	XP_024308862.1:p.Ser21894Ala
XM_024453095.1:c.65677T>G (TTN)	XP_024308863.1:p.Ser21893Ala
XM_024453096.1:c.65110T>G (TTN)	XP_024308864.1:p.Ser21704Ala
XM_024453097.1:c.62452T>G (TTN)	XP_024308865.1:p.Ser20818Ala
XM_024453098.1:c.62371T>G (TTN)	XP_024308866.1:p.Ser20791Ala
XM_024453099.1:c.44134T>G (TTN)	XP_024308867.1:p.Ser14712Ala
XM_024453100.1:c.33988T>G (TTN)	XP_024308868.1:p.Ser11330Ala