Canonical Allele Identifier: CA349543306

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179424365T>G (hg19) ; chr2:g.178559638T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178559638T>G , CM000664.2:g.178559638T>G	GRCh38
NC_000002.11:g.179424365T>G , CM000664.1:g.179424365T>G	GRCh37
NC_000002.10:g.179132611T>G	NCBI36
NG_011618.3:g.276165A>C , LRG_391:g.276165A>C
NG_051363.1:g.41812T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.78790A>C (TTN)	ENSP00000343764.6:p.Ser26264Arg
ENST00000342175.11:c.59875A>C (TTN)	ENSP00000340554.6:p.Ser19959Arg
ENST00000359218.10:c.59674A>C (TTN)	ENSP00000352154.5:p.Ser19892Arg
ENST00000342175.10:c.59875A>C (TTN)	ENSP00000340554.6:p.Ser19959Arg
ENST00000342992.10:c.78790A>C (TTN)	ENSP00000343764.6:p.Ser26264Arg
ENST00000359218.9:c.59674A>C (TTN)	ENSP00000352154.5:p.Ser19892Arg
ENST00000460472.6:c.59299A>C (TTN)	ENSP00000434586.1:p.Ser19767Arg
ENST00000589042.5:c.86494A>C (TTN) MANE Select	ENSP00000467141.1:p.Ser28832Arg
ENST00000591111.5:c.81571A>C (TTN)	ENSP00000465570.1:p.Ser27191Arg
ENST00000615779.4:c.81571A>C (TTN)	ENSP00000483597.1:p.Ser27191Arg
NM_001256850.1:c.81571A>C (TTN)	NP_001243779.1:p.Ser27191Arg
NM_001267550.2:c.86494A>C (TTN) MANE Select	NP_001254479.2:p.Ser28832Arg
NM_003319.4:c.59299A>C (TTN)	NP_003310.4:p.Ser19767Arg
NM_133378.4:c.78790A>C (TTN)	NP_596869.4:p.Ser26264Arg
NM_133432.3:c.59674A>C (TTN)	NP_597676.3:p.Ser19892Arg
NM_133437.4:c.59875A>C (TTN)	NP_597681.4:p.Ser19959Arg
NR_038271.1:n.447-11662T>G (TTN-AS1)
NR_038272.1:n.2043+17277T>G (TTN-AS1)
XM_011511729.1:c.85591A>C (TTN)	XP_011510031.1:p.Ser28531Arg
XM_011511730.1:c.59485A>C (TTN)	XP_011510032.1:p.Ser19829Arg
XM_011511731.1:c.59344A>C (TTN)	XP_011510033.1:p.Ser19782Arg
XM_017004819.1:c.85387A>C (TTN)	XP_016860308.1:p.Ser28463Arg
XM_017004820.1:c.80785A>C (TTN)	XP_016860309.1:p.Ser26929Arg
XM_017004821.1:c.80782A>C (TTN)	XP_016860310.1:p.Ser26928Arg
XM_017004822.1:c.77824A>C (TTN)	XP_016860311.1:p.Ser25942Arg
XM_017004823.1:c.59440A>C (TTN)	XP_016860312.1:p.Ser19814Arg
XM_024453094.1:c.80935A>C (TTN)	XP_024308862.1:p.Ser26979Arg
XM_024453095.1:c.80932A>C (TTN)	XP_024308863.1:p.Ser26978Arg
XM_024453096.1:c.80365A>C (TTN)	XP_024308864.1:p.Ser26789Arg
XM_024453097.1:c.77707A>C (TTN)	XP_024308865.1:p.Ser25903Arg
XM_024453098.1:c.77626A>C (TTN)	XP_024308866.1:p.Ser25876Arg
XM_024453099.1:c.59389A>C (TTN)	XP_024308867.1:p.Ser19797Arg
XM_024453100.1:c.49243A>C (TTN)	XP_024308868.1:p.Ser16415Arg