Canonical Allele Identifier: CA430235487

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395319G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530592G>A , CM000664.2:g.178530592G>A	GRCh38
NC_000002.11:g.179395319G>A , CM000664.1:g.179395319G>A	GRCh37
NC_000002.10:g.179103565G>A	NCBI36
NG_011618.3:g.305211C>T , LRG_391:g.305211C>T
NG_051363.1:g.12766G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98319C>T (TTN)	ENSP00000343764.6:p.Thr32773=
ENST00000342175.11:c.79404C>T (TTN)	ENSP00000340554.6:p.Thr26468=
ENST00000359218.10:c.79203C>T (TTN)	ENSP00000352154.5:p.Thr26401=
ENST00000342175.10:c.79404C>T (TTN)	ENSP00000340554.6:p.Thr26468=
ENST00000342992.10:c.98319C>T (TTN)	ENSP00000343764.6:p.Thr32773=
ENST00000359218.9:c.79203C>T (TTN)	ENSP00000352154.5:p.Thr26401=
ENST00000460472.6:c.78828C>T (TTN)	ENSP00000434586.1:p.Thr26276=
ENST00000589042.5:c.106023C>T (TTN) MANE Select	ENSP00000467141.1:p.Thr35341=
ENST00000591111.5:c.101100C>T (TTN)	ENSP00000465570.1:p.Thr33700=
ENST00000615779.4:c.101100C>T (TTN)	ENSP00000483597.1:p.Thr33700=
NM_001256850.1:c.101100C>T (TTN)	NP_001243779.1:p.Thr33700=
NM_001267550.2:c.106023C>T (TTN) MANE Select	NP_001254479.2:p.Thr35341=
NM_003319.4:c.78828C>T (TTN)	NP_003310.4:p.Thr26276=
NM_133378.4:c.98319C>T (TTN)	NP_596869.4:p.Thr32773=
NM_133432.3:c.79203C>T (TTN)	NP_597676.3:p.Thr26401=
NM_133437.4:c.79404C>T (TTN)	NP_597681.4:p.Thr26468=
NR_038271.1:n.446+6956G>A (TTN-AS1)
NR_038272.1:n.220-5140G>A (TTN-AS1)
XM_011511729.1:c.105120C>T (TTN)	XP_011510031.1:p.Thr35040=
XM_011511730.1:c.79014C>T (TTN)	XP_011510032.1:p.Thr26338=
XM_011511731.1:c.78873C>T (TTN)	XP_011510033.1:p.Thr26291=
XM_017004819.1:c.104916C>T (TTN)	XP_016860308.1:p.Thr34972=
XM_017004820.1:c.100314C>T (TTN)	XP_016860309.1:p.Thr33438=
XM_017004821.1:c.100311C>T (TTN)	XP_016860310.1:p.Thr33437=
XM_017004822.1:c.97353C>T (TTN)	XP_016860311.1:p.Thr32451=
XM_017004823.1:c.78969C>T (TTN)	XP_016860312.1:p.Thr26323=
XM_024453094.1:c.100464C>T (TTN)	XP_024308862.1:p.Thr33488=
XM_024453095.1:c.100461C>T (TTN)	XP_024308863.1:p.Thr33487=
XM_024453096.1:c.99894C>T (TTN)	XP_024308864.1:p.Thr33298=
XM_024453097.1:c.97236C>T (TTN)	XP_024308865.1:p.Thr32412=
XM_024453098.1:c.97155C>T (TTN)	XP_024308866.1:p.Thr32385=
XM_024453099.1:c.78918C>T (TTN)	XP_024308867.1:p.Thr26306=
XM_024453100.1:c.68772C>T (TTN)	XP_024308868.1:p.Thr22924=