Canonical Allele Identifier: CA349536897

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179422712A>C (hg19) ; chr2:g.178557985A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557985A>C , CM000664.2:g.178557985A>C	GRCh38
NC_000002.11:g.179422712A>C , CM000664.1:g.179422712A>C	GRCh37
NC_000002.10:g.179130958A>C	NCBI36
NG_011618.3:g.277818T>G , LRG_391:g.277818T>G
NG_051363.1:g.40159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.79665T>G (TTN)	ENSP00000343764.6:p.Ser26555Arg
ENST00000342175.11:c.60750T>G (TTN)	ENSP00000340554.6:p.Ser20250Arg
ENST00000359218.10:c.60549T>G (TTN)	ENSP00000352154.5:p.Ser20183Arg
ENST00000342175.10:c.60750T>G (TTN)	ENSP00000340554.6:p.Ser20250Arg
ENST00000342992.10:c.79665T>G (TTN)	ENSP00000343764.6:p.Ser26555Arg
ENST00000359218.9:c.60549T>G (TTN)	ENSP00000352154.5:p.Ser20183Arg
ENST00000460472.6:c.60174T>G (TTN)	ENSP00000434586.1:p.Ser20058Arg
ENST00000589042.5:c.87369T>G (TTN) MANE Select	ENSP00000467141.1:p.Ser29123Arg
ENST00000591111.5:c.82446T>G (TTN)	ENSP00000465570.1:p.Ser27482Arg
ENST00000615779.4:c.82446T>G (TTN)	ENSP00000483597.1:p.Ser27482Arg
NM_001256850.1:c.82446T>G (TTN)	NP_001243779.1:p.Ser27482Arg
NM_001267550.2:c.87369T>G (TTN) MANE Select	NP_001254479.2:p.Ser29123Arg
NM_003319.4:c.60174T>G (TTN)	NP_003310.4:p.Ser20058Arg
NM_133378.4:c.79665T>G (TTN)	NP_596869.4:p.Ser26555Arg
NM_133432.3:c.60549T>G (TTN)	NP_597676.3:p.Ser20183Arg
NM_133437.4:c.60750T>G (TTN)	NP_597681.4:p.Ser20250Arg
NR_038271.1:n.447-13315A>C (TTN-AS1)
NR_038272.1:n.2043+15624A>C (TTN-AS1)
XM_011511729.1:c.86466T>G (TTN)	XP_011510031.1:p.Ser28822Arg
XM_011511730.1:c.60360T>G (TTN)	XP_011510032.1:p.Ser20120Arg
XM_011511731.1:c.60219T>G (TTN)	XP_011510033.1:p.Ser20073Arg
XM_017004819.1:c.86262T>G (TTN)	XP_016860308.1:p.Ser28754Arg
XM_017004820.1:c.81660T>G (TTN)	XP_016860309.1:p.Ser27220Arg
XM_017004821.1:c.81657T>G (TTN)	XP_016860310.1:p.Ser27219Arg
XM_017004822.1:c.78699T>G (TTN)	XP_016860311.1:p.Ser26233Arg
XM_017004823.1:c.60315T>G (TTN)	XP_016860312.1:p.Ser20105Arg
XM_024453094.1:c.81810T>G (TTN)	XP_024308862.1:p.Ser27270Arg
XM_024453095.1:c.81807T>G (TTN)	XP_024308863.1:p.Ser27269Arg
XM_024453096.1:c.81240T>G (TTN)	XP_024308864.1:p.Ser27080Arg
XM_024453097.1:c.78582T>G (TTN)	XP_024308865.1:p.Ser26194Arg
XM_024453098.1:c.78501T>G (TTN)	XP_024308866.1:p.Ser26167Arg
XM_024453099.1:c.60264T>G (TTN)	XP_024308867.1:p.Ser20088Arg
XM_024453100.1:c.50118T>G (TTN)	XP_024308868.1:p.Ser16706Arg