Canonical Allele Identifier: CA349405439

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394805G>T (hg19) ; chr2:g.178530078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530078G>T , CM000664.2:g.178530078G>T	GRCh38
NC_000002.11:g.179394805G>T , CM000664.1:g.179394805G>T	GRCh37
NC_000002.10:g.179103051G>T	NCBI36
NG_011618.3:g.305725C>A , LRG_391:g.305725C>A
NG_051363.1:g.12252G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98709C>A (TTN)	ENSP00000343764.6:p.Asp32903Glu
ENST00000342175.11:c.79794C>A (TTN)	ENSP00000340554.6:p.Asp26598Glu
ENST00000359218.10:c.79593C>A (TTN)	ENSP00000352154.5:p.Asp26531Glu
ENST00000342175.10:c.79794C>A (TTN)	ENSP00000340554.6:p.Asp26598Glu
ENST00000342992.10:c.98709C>A (TTN)	ENSP00000343764.6:p.Asp32903Glu
ENST00000359218.9:c.79593C>A (TTN)	ENSP00000352154.5:p.Asp26531Glu
ENST00000460472.6:c.79218C>A (TTN)	ENSP00000434586.1:p.Asp26406Glu
ENST00000589042.5:c.106413C>A (TTN) MANE Select	ENSP00000467141.1:p.Asp35471Glu
ENST00000591111.5:c.101490C>A (TTN)	ENSP00000465570.1:p.Asp33830Glu
ENST00000615779.4:c.101490C>A (TTN)	ENSP00000483597.1:p.Asp33830Glu
NM_001256850.1:c.101490C>A (TTN)	NP_001243779.1:p.Asp33830Glu
NM_001267550.2:c.106413C>A (TTN) MANE Select	NP_001254479.2:p.Asp35471Glu
NM_003319.4:c.79218C>A (TTN)	NP_003310.4:p.Asp26406Glu
NM_133378.4:c.98709C>A (TTN)	NP_596869.4:p.Asp32903Glu
NM_133432.3:c.79593C>A (TTN)	NP_597676.3:p.Asp26531Glu
NM_133437.4:c.79794C>A (TTN)	NP_597681.4:p.Asp26598Glu
NR_038271.1:n.446+6442G>T (TTN-AS1)
NR_038272.1:n.220-5654G>T (TTN-AS1)
XM_011511729.1:c.105510C>A (TTN)	XP_011510031.1:p.Asp35170Glu
XM_011511730.1:c.79404C>A (TTN)	XP_011510032.1:p.Asp26468Glu
XM_011511731.1:c.79263C>A (TTN)	XP_011510033.1:p.Asp26421Glu
XM_017004819.1:c.105306C>A (TTN)	XP_016860308.1:p.Asp35102Glu
XM_017004820.1:c.100704C>A (TTN)	XP_016860309.1:p.Asp33568Glu
XM_017004821.1:c.100701C>A (TTN)	XP_016860310.1:p.Asp33567Glu
XM_017004822.1:c.97743C>A (TTN)	XP_016860311.1:p.Asp32581Glu
XM_017004823.1:c.79359C>A (TTN)	XP_016860312.1:p.Asp26453Glu
XM_024453094.1:c.100854C>A (TTN)	XP_024308862.1:p.Asp33618Glu
XM_024453095.1:c.100851C>A (TTN)	XP_024308863.1:p.Asp33617Glu
XM_024453096.1:c.100284C>A (TTN)	XP_024308864.1:p.Asp33428Glu
XM_024453097.1:c.97626C>A (TTN)	XP_024308865.1:p.Asp32542Glu
XM_024453098.1:c.97545C>A (TTN)	XP_024308866.1:p.Asp32515Glu
XM_024453099.1:c.79308C>A (TTN)	XP_024308867.1:p.Asp26436Glu
XM_024453100.1:c.69162C>A (TTN)	XP_024308868.1:p.Asp23054Glu