Canonical Allele Identifier: CA349495577

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414501C>G (hg19) ; chr2:g.178549774C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549774C>G , CM000664.2:g.178549774C>G	GRCh38
NC_000002.11:g.179414501C>G , CM000664.1:g.179414501C>G	GRCh37
NC_000002.10:g.179122747C>G	NCBI36
NG_011618.3:g.286029G>C , LRG_391:g.286029G>C
NG_051363.1:g.31948C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84244G>C (TTN)	ENSP00000343764.6:p.Ala28082Pro
ENST00000342175.11:c.65329G>C (TTN)	ENSP00000340554.6:p.Ala21777Pro
ENST00000359218.10:c.65128G>C (TTN)	ENSP00000352154.5:p.Ala21710Pro
ENST00000342175.10:c.65329G>C (TTN)	ENSP00000340554.6:p.Ala21777Pro
ENST00000342992.10:c.84244G>C (TTN)	ENSP00000343764.6:p.Ala28082Pro
ENST00000359218.9:c.65128G>C (TTN)	ENSP00000352154.5:p.Ala21710Pro
ENST00000460472.6:c.64753G>C (TTN)	ENSP00000434586.1:p.Ala21585Pro
ENST00000589042.5:c.91948G>C (TTN) MANE Select	ENSP00000467141.1:p.Ala30650Pro
ENST00000591111.5:c.87025G>C (TTN)	ENSP00000465570.1:p.Ala29009Pro
ENST00000615779.4:c.87025G>C (TTN)	ENSP00000483597.1:p.Ala29009Pro
NM_001256850.1:c.87025G>C (TTN)	NP_001243779.1:p.Ala29009Pro
NM_001267550.2:c.91948G>C (TTN) MANE Select	NP_001254479.2:p.Ala30650Pro
NM_003319.4:c.64753G>C (TTN)	NP_003310.4:p.Ala21585Pro
NM_133378.4:c.84244G>C (TTN)	NP_596869.4:p.Ala28082Pro
NM_133432.3:c.65128G>C (TTN)	NP_597676.3:p.Ala21710Pro
NM_133437.4:c.65329G>C (TTN)	NP_597681.4:p.Ala21777Pro
NR_038271.1:n.447-21526C>G (TTN-AS1)
NR_038272.1:n.2043+7413C>G (TTN-AS1)
XM_011511729.1:c.91045G>C (TTN)	XP_011510031.1:p.Ala30349Pro
XM_011511730.1:c.64939G>C (TTN)	XP_011510032.1:p.Ala21647Pro
XM_011511731.1:c.64798G>C (TTN)	XP_011510033.1:p.Ala21600Pro
XM_017004819.1:c.90841G>C (TTN)	XP_016860308.1:p.Ala30281Pro
XM_017004820.1:c.86239G>C (TTN)	XP_016860309.1:p.Ala28747Pro
XM_017004821.1:c.86236G>C (TTN)	XP_016860310.1:p.Ala28746Pro
XM_017004822.1:c.83278G>C (TTN)	XP_016860311.1:p.Ala27760Pro
XM_017004823.1:c.64894G>C (TTN)	XP_016860312.1:p.Ala21632Pro
XM_024453094.1:c.86389G>C (TTN)	XP_024308862.1:p.Ala28797Pro
XM_024453095.1:c.86386G>C (TTN)	XP_024308863.1:p.Ala28796Pro
XM_024453096.1:c.85819G>C (TTN)	XP_024308864.1:p.Ala28607Pro
XM_024453097.1:c.83161G>C (TTN)	XP_024308865.1:p.Ala27721Pro
XM_024453098.1:c.83080G>C (TTN)	XP_024308866.1:p.Ala27694Pro
XM_024453099.1:c.64843G>C (TTN)	XP_024308867.1:p.Ala21615Pro
XM_024453100.1:c.54697G>C (TTN)	XP_024308868.1:p.Ala18233Pro