Canonical Allele Identifier: CA349600894

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179432014T>C (hg19) ; chr2:g.178567287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178567287T>C , CM000664.2:g.178567287T>C	GRCh38
NC_000002.11:g.179432014T>C , CM000664.1:g.179432014T>C	GRCh37
NC_000002.10:g.179140260T>C	NCBI36
NG_011618.3:g.268516A>G , LRG_391:g.268516A>G
NG_051363.1:g.49461T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.71141A>G (TTN)	ENSP00000343764.6:p.Lys23714Arg
ENST00000342175.11:c.52226A>G (TTN)	ENSP00000340554.6:p.Lys17409Arg
ENST00000359218.10:c.52025A>G (TTN)	ENSP00000352154.5:p.Lys17342Arg
ENST00000342175.10:c.52226A>G (TTN)	ENSP00000340554.6:p.Lys17409Arg
ENST00000342992.10:c.71141A>G (TTN)	ENSP00000343764.6:p.Lys23714Arg
ENST00000359218.9:c.52025A>G (TTN)	ENSP00000352154.5:p.Lys17342Arg
ENST00000460472.6:c.51650A>G (TTN)	ENSP00000434586.1:p.Lys17217Arg
ENST00000589042.5:c.78845A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys26282Arg
ENST00000591111.5:c.73922A>G (TTN)	ENSP00000465570.1:p.Lys24641Arg
ENST00000615779.4:c.73922A>G (TTN)	ENSP00000483597.1:p.Lys24641Arg
NM_001256850.1:c.73922A>G (TTN)	NP_001243779.1:p.Lys24641Arg
NM_001267550.2:c.78845A>G (TTN) MANE Select	NP_001254479.2:p.Lys26282Arg
NM_003319.4:c.51650A>G (TTN)	NP_003310.4:p.Lys17217Arg
NM_133378.4:c.71141A>G (TTN)	NP_596869.4:p.Lys23714Arg
NM_133432.3:c.52025A>G (TTN)	NP_597676.3:p.Lys17342Arg
NM_133437.4:c.52226A>G (TTN)	NP_597681.4:p.Lys17409Arg
NR_038271.1:n.447-4013T>C (TTN-AS1)
NR_038272.1:n.2044-15285T>C (TTN-AS1)
XM_011511729.1:c.77942A>G (TTN)	XP_011510031.1:p.Lys25981Arg
XM_011511730.1:c.51836A>G (TTN)	XP_011510032.1:p.Lys17279Arg
XM_011511731.1:c.51695A>G (TTN)	XP_011510033.1:p.Lys17232Arg
XM_017004819.1:c.77738A>G (TTN)	XP_016860308.1:p.Lys25913Arg
XM_017004820.1:c.73136A>G (TTN)	XP_016860309.1:p.Lys24379Arg
XM_017004821.1:c.73133A>G (TTN)	XP_016860310.1:p.Lys24378Arg
XM_017004822.1:c.70175A>G (TTN)	XP_016860311.1:p.Lys23392Arg
XM_017004823.1:c.51791A>G (TTN)	XP_016860312.1:p.Lys17264Arg
XM_024453094.1:c.73286A>G (TTN)	XP_024308862.1:p.Lys24429Arg
XM_024453095.1:c.73283A>G (TTN)	XP_024308863.1:p.Lys24428Arg
XM_024453096.1:c.72716A>G (TTN)	XP_024308864.1:p.Lys24239Arg
XM_024453097.1:c.70058A>G (TTN)	XP_024308865.1:p.Lys23353Arg
XM_024453098.1:c.69977A>G (TTN)	XP_024308866.1:p.Lys23326Arg
XM_024453099.1:c.51740A>G (TTN)	XP_024308867.1:p.Lys17247Arg
XM_024453100.1:c.41594A>G (TTN)	XP_024308868.1:p.Lys13865Arg