Canonical Allele Identifier: CA430276087

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179486374T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621647T>A , CM000664.2:g.178621647T>A	GRCh38
NC_000002.11:g.179486374T>A , CM000664.1:g.179486374T>A	GRCh37
NC_000002.10:g.179194619T>A	NCBI36
NG_011618.3:g.214156A>T , LRG_391:g.214156A>T
NG_051363.1:g.103821T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37473A>T	ENSP00000343764.6:p.Ala12491=
ENST00000342175.11:c.18558A>T	ENSP00000340554.6:p.Ala6186=
ENST00000359218.10:c.18357A>T	ENSP00000352154.5:p.Ala6119=
ENST00000342175.10:c.18558A>T	ENSP00000340554.6:p.Ala6186=
ENST00000342992.10:c.37473A>T	ENSP00000343764.6:p.Ala12491=
ENST00000359218.9:c.18357A>T	ENSP00000352154.5:p.Ala6119=
ENST00000460472.6:c.17982A>T	ENSP00000434586.1:p.Ala5994=
ENST00000589042.5:c.45177A>T MANE Select	ENSP00000467141.1:p.Ala15059=
ENST00000591111.5:c.40254A>T	ENSP00000465570.1:p.Ala13418=
ENST00000615779.4:c.40254A>T	ENSP00000483597.1:p.Ala13418=
NM_001256850.1:c.40254A>T	NP_001243779.1:p.Ala13418=
NM_001267550.2:c.45177A>T MANE Select	NP_001254479.2:p.Ala15059=
NM_003319.4:c.17982A>T	NP_003310.4:p.Ala5994=
NM_133378.4:c.37473A>T	NP_596869.4:p.Ala12491=
NM_133432.3:c.18357A>T	NP_597676.3:p.Ala6119=
NM_133437.4:c.18558A>T	NP_597681.4:p.Ala6186=
XM_011511729.1:c.44274A>T	XP_011510031.1:p.Ala14758=
XM_011511730.1:c.18168A>T	XP_011510032.1:p.Ala6056=
XM_011511731.1:c.18027A>T	XP_011510033.1:p.Ala6009=
XM_017004819.1:c.44070A>T	XP_016860308.1:p.Ala14690=
XM_017004820.1:c.39468A>T	XP_016860309.1:p.Ala13156=
XM_017004821.1:c.39465A>T	XP_016860310.1:p.Ala13155=
XM_017004822.1:c.36507A>T	XP_016860311.1:p.Ala12169=
XM_017004823.1:c.18123A>T	XP_016860312.1:p.Ala6041=
XM_024453094.1:c.39618A>T	XP_024308862.1:p.Ala13206=
XM_024453095.1:c.39615A>T	XP_024308863.1:p.Ala13205=
XM_024453096.1:c.39048A>T	XP_024308864.1:p.Ala13016=
XM_024453097.1:c.36390A>T	XP_024308865.1:p.Ala12130=
XM_024453098.1:c.36309A>T	XP_024308866.1:p.Ala12103=
XM_024453099.1:c.18072A>T	XP_024308867.1:p.Ala6024=
XM_024453100.1:c.7926A>T	XP_024308868.1:p.Ala2642=