Canonical Allele Identifier: CA349398536

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179391836T>A (hg19) ; chr2:g.178527109T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527109T>A , CM000664.2:g.178527109T>A	GRCh38
NC_000002.11:g.179391836T>A , CM000664.1:g.179391836T>A	GRCh37
NC_000002.10:g.179100082T>A	NCBI36
NG_011618.3:g.308694A>T , LRG_391:g.308694A>T
NG_051363.1:g.9283T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100175A>T (TTN)	ENSP00000343764.6:p.Asp33392Val
ENST00000342175.11:c.81260A>T (TTN)	ENSP00000340554.6:p.Asp27087Val
ENST00000359218.10:c.81059A>T (TTN)	ENSP00000352154.5:p.Asp27020Val
ENST00000342175.10:c.81260A>T (TTN)	ENSP00000340554.6:p.Asp27087Val
ENST00000342992.10:c.100175A>T (TTN)	ENSP00000343764.6:p.Asp33392Val
ENST00000359218.9:c.81059A>T (TTN)	ENSP00000352154.5:p.Asp27020Val
ENST00000460472.6:c.80684A>T (TTN)	ENSP00000434586.1:p.Asp26895Val
ENST00000589042.5:c.107879A>T (TTN) MANE Select	ENSP00000467141.1:p.Asp35960Val
ENST00000591111.5:c.102956A>T (TTN)	ENSP00000465570.1:p.Asp34319Val
ENST00000615779.4:c.102956A>T (TTN)	ENSP00000483597.1:p.Asp34319Val
NM_001256850.1:c.102956A>T (TTN)	NP_001243779.1:p.Asp34319Val
NM_001267550.2:c.107879A>T (TTN) MANE Select	NP_001254479.2:p.Asp35960Val
NM_003319.4:c.80684A>T (TTN)	NP_003310.4:p.Asp26895Val
NM_133378.4:c.100175A>T (TTN)	NP_596869.4:p.Asp33392Val
NM_133432.3:c.81059A>T (TTN)	NP_597676.3:p.Asp27020Val
NM_133437.4:c.81260A>T (TTN)	NP_597681.4:p.Asp27087Val
NR_038271.1:n.446+3473T>A (TTN-AS1)
NR_038272.1:n.219+3473T>A (TTN-AS1)
XM_011511729.1:c.106976A>T (TTN)	XP_011510031.1:p.Asp35659Val
XM_011511730.1:c.80870A>T (TTN)	XP_011510032.1:p.Asp26957Val
XM_011511731.1:c.80729A>T (TTN)	XP_011510033.1:p.Asp26910Val
XM_017004819.1:c.106772A>T (TTN)	XP_016860308.1:p.Asp35591Val
XM_017004820.1:c.102170A>T (TTN)	XP_016860309.1:p.Asp34057Val
XM_017004821.1:c.102167A>T (TTN)	XP_016860310.1:p.Asp34056Val
XM_017004822.1:c.99209A>T (TTN)	XP_016860311.1:p.Asp33070Val
XM_017004823.1:c.80825A>T (TTN)	XP_016860312.1:p.Asp26942Val
XM_024453094.1:c.102320A>T (TTN)	XP_024308862.1:p.Asp34107Val
XM_024453095.1:c.102317A>T (TTN)	XP_024308863.1:p.Asp34106Val
XM_024453096.1:c.101750A>T (TTN)	XP_024308864.1:p.Asp33917Val
XM_024453097.1:c.99092A>T (TTN)	XP_024308865.1:p.Asp33031Val
XM_024453098.1:c.99011A>T (TTN)	XP_024308866.1:p.Asp33004Val
XM_024453099.1:c.80774A>T (TTN)	XP_024308867.1:p.Asp26925Val
XM_024453100.1:c.70628A>T (TTN)	XP_024308868.1:p.Asp23543Val