Canonical Allele Identifier: CA349405524

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394819T>C (hg19) ; chr2:g.178530092T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530092T>C , CM000664.2:g.178530092T>C	GRCh38
NC_000002.11:g.179394819T>C , CM000664.1:g.179394819T>C	GRCh37
NC_000002.10:g.179103065T>C	NCBI36
NG_011618.3:g.305711A>G , LRG_391:g.305711A>G
NG_051363.1:g.12266T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98695A>G (TTN)	ENSP00000343764.6:p.Lys32899Glu
ENST00000342175.11:c.79780A>G (TTN)	ENSP00000340554.6:p.Lys26594Glu
ENST00000359218.10:c.79579A>G (TTN)	ENSP00000352154.5:p.Lys26527Glu
ENST00000342175.10:c.79780A>G (TTN)	ENSP00000340554.6:p.Lys26594Glu
ENST00000342992.10:c.98695A>G (TTN)	ENSP00000343764.6:p.Lys32899Glu
ENST00000359218.9:c.79579A>G (TTN)	ENSP00000352154.5:p.Lys26527Glu
ENST00000460472.6:c.79204A>G (TTN)	ENSP00000434586.1:p.Lys26402Glu
ENST00000589042.5:c.106399A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35467Glu
ENST00000591111.5:c.101476A>G (TTN)	ENSP00000465570.1:p.Lys33826Glu
ENST00000615779.4:c.101476A>G (TTN)	ENSP00000483597.1:p.Lys33826Glu
NM_001256850.1:c.101476A>G (TTN)	NP_001243779.1:p.Lys33826Glu
NM_001267550.2:c.106399A>G (TTN) MANE Select	NP_001254479.2:p.Lys35467Glu
NM_003319.4:c.79204A>G (TTN)	NP_003310.4:p.Lys26402Glu
NM_133378.4:c.98695A>G (TTN)	NP_596869.4:p.Lys32899Glu
NM_133432.3:c.79579A>G (TTN)	NP_597676.3:p.Lys26527Glu
NM_133437.4:c.79780A>G (TTN)	NP_597681.4:p.Lys26594Glu
NR_038271.1:n.446+6456T>C (TTN-AS1)
NR_038272.1:n.220-5640T>C (TTN-AS1)
XM_011511729.1:c.105496A>G (TTN)	XP_011510031.1:p.Lys35166Glu
XM_011511730.1:c.79390A>G (TTN)	XP_011510032.1:p.Lys26464Glu
XM_011511731.1:c.79249A>G (TTN)	XP_011510033.1:p.Lys26417Glu
XM_017004819.1:c.105292A>G (TTN)	XP_016860308.1:p.Lys35098Glu
XM_017004820.1:c.100690A>G (TTN)	XP_016860309.1:p.Lys33564Glu
XM_017004821.1:c.100687A>G (TTN)	XP_016860310.1:p.Lys33563Glu
XM_017004822.1:c.97729A>G (TTN)	XP_016860311.1:p.Lys32577Glu
XM_017004823.1:c.79345A>G (TTN)	XP_016860312.1:p.Lys26449Glu
XM_024453094.1:c.100840A>G (TTN)	XP_024308862.1:p.Lys33614Glu
XM_024453095.1:c.100837A>G (TTN)	XP_024308863.1:p.Lys33613Glu
XM_024453096.1:c.100270A>G (TTN)	XP_024308864.1:p.Lys33424Glu
XM_024453097.1:c.97612A>G (TTN)	XP_024308865.1:p.Lys32538Glu
XM_024453098.1:c.97531A>G (TTN)	XP_024308866.1:p.Lys32511Glu
XM_024453099.1:c.79294A>G (TTN)	XP_024308867.1:p.Lys26432Glu
XM_024453100.1:c.69148A>G (TTN)	XP_024308868.1:p.Lys23050Glu