Canonical Allele Identifier: CA349406665

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395147T>C (hg19) ; chr2:g.178530420T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530420T>C , CM000664.2:g.178530420T>C	GRCh38
NC_000002.11:g.179395147T>C , CM000664.1:g.179395147T>C	GRCh37
NC_000002.10:g.179103393T>C	NCBI36
NG_011618.3:g.305383A>G , LRG_391:g.305383A>G
NG_051363.1:g.12594T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98491A>G (TTN)	ENSP00000343764.6:p.Thr32831Ala
ENST00000342175.11:c.79576A>G (TTN)	ENSP00000340554.6:p.Thr26526Ala
ENST00000359218.10:c.79375A>G (TTN)	ENSP00000352154.5:p.Thr26459Ala
ENST00000342175.10:c.79576A>G (TTN)	ENSP00000340554.6:p.Thr26526Ala
ENST00000342992.10:c.98491A>G (TTN)	ENSP00000343764.6:p.Thr32831Ala
ENST00000359218.9:c.79375A>G (TTN)	ENSP00000352154.5:p.Thr26459Ala
ENST00000460472.6:c.79000A>G (TTN)	ENSP00000434586.1:p.Thr26334Ala
ENST00000589042.5:c.106195A>G (TTN) MANE Select	ENSP00000467141.1:p.Thr35399Ala
ENST00000591111.5:c.101272A>G (TTN)	ENSP00000465570.1:p.Thr33758Ala
ENST00000615779.4:c.101272A>G (TTN)	ENSP00000483597.1:p.Thr33758Ala
NM_001256850.1:c.101272A>G (TTN)	NP_001243779.1:p.Thr33758Ala
NM_001267550.2:c.106195A>G (TTN) MANE Select	NP_001254479.2:p.Thr35399Ala
NM_003319.4:c.79000A>G (TTN)	NP_003310.4:p.Thr26334Ala
NM_133378.4:c.98491A>G (TTN)	NP_596869.4:p.Thr32831Ala
NM_133432.3:c.79375A>G (TTN)	NP_597676.3:p.Thr26459Ala
NM_133437.4:c.79576A>G (TTN)	NP_597681.4:p.Thr26526Ala
NR_038271.1:n.446+6784T>C (TTN-AS1)
NR_038272.1:n.220-5312T>C (TTN-AS1)
XM_011511729.1:c.105292A>G (TTN)	XP_011510031.1:p.Thr35098Ala
XM_011511730.1:c.79186A>G (TTN)	XP_011510032.1:p.Thr26396Ala
XM_011511731.1:c.79045A>G (TTN)	XP_011510033.1:p.Thr26349Ala
XM_017004819.1:c.105088A>G (TTN)	XP_016860308.1:p.Thr35030Ala
XM_017004820.1:c.100486A>G (TTN)	XP_016860309.1:p.Thr33496Ala
XM_017004821.1:c.100483A>G (TTN)	XP_016860310.1:p.Thr33495Ala
XM_017004822.1:c.97525A>G (TTN)	XP_016860311.1:p.Thr32509Ala
XM_017004823.1:c.79141A>G (TTN)	XP_016860312.1:p.Thr26381Ala
XM_024453094.1:c.100636A>G (TTN)	XP_024308862.1:p.Thr33546Ala
XM_024453095.1:c.100633A>G (TTN)	XP_024308863.1:p.Thr33545Ala
XM_024453096.1:c.100066A>G (TTN)	XP_024308864.1:p.Thr33356Ala
XM_024453097.1:c.97408A>G (TTN)	XP_024308865.1:p.Thr32470Ala
XM_024453098.1:c.97327A>G (TTN)	XP_024308866.1:p.Thr32443Ala
XM_024453099.1:c.79090A>G (TTN)	XP_024308867.1:p.Thr26364Ala
XM_024453100.1:c.68944A>G (TTN)	XP_024308868.1:p.Thr22982Ala