Canonical Allele Identifier: CA430295008

Gene: TTN

Linked Data

• dbSNP Id: rs1425281282
• gnomAD v2: 2-179602888-C-T
• MyVariant Identifiers: chr2:g.179602888C>T (hg19) ; chr2:g.178738161C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178738161C>T , CM000664.2:g.178738161C>T	GRCh38
NC_000002.11:g.179602888C>T , CM000664.1:g.179602888C>T	GRCh37
NC_000002.10:g.179311133C>T	NCBI36
NG_011618.3:g.97642G>A , LRG_391:g.97642G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.10560G>A	ENSP00000343764.6:p.Val3520=
ENST00000342175.11:c.13779G>A	ENSP00000340554.6:p.Val4593=
ENST00000359218.10:c.13578G>A	ENSP00000352154.5:p.Val4526=
ENST00000342175.10:c.13779G>A	ENSP00000340554.6:p.Val4593=
ENST00000342992.10:c.10560G>A	ENSP00000343764.6:p.Val3520=
ENST00000359218.9:c.13578G>A	ENSP00000352154.5:p.Val4526=
ENST00000460472.6:c.13203G>A	ENSP00000434586.1:p.Val4401=
ENST00000589042.5:c.14292G>A MANE Select	ENSP00000467141.1:p.Val4764=
ENST00000591111.5:c.13341G>A	ENSP00000465570.1:p.Val4447=
ENST00000615779.4:c.13341G>A	ENSP00000483597.1:p.Val4447=
NM_001256850.1:c.13341G>A	NP_001243779.1:p.Val4447=
NM_001267550.2:c.14292G>A MANE Select	NP_001254479.2:p.Val4764=
NM_003319.4:c.13203G>A	NP_003310.4:p.Val4401=
NM_133378.4:c.10560G>A	NP_596869.4:p.Val3520=
NM_133432.3:c.13578G>A	NP_597676.3:p.Val4526=
NM_133437.4:c.13779G>A	NP_597681.4:p.Val4593=
XM_011511729.1:c.13389G>A	XP_011510031.1:p.Val4463=
XM_011511730.1:c.13389G>A	XP_011510032.1:p.Val4463=
XM_011511731.1:c.13248G>A	XP_011510033.1:p.Val4416=
XM_017004819.1:c.13344G>A	XP_016860308.1:p.Val4448=
XM_017004820.1:c.10563G>A	XP_016860309.1:p.Val3521=
XM_017004821.1:c.10560G>A	XP_016860310.1:p.Val3520=
XM_017004822.1:c.13344G>A	XP_016860311.1:p.Val4448=
XM_017004823.1:c.13344G>A	XP_016860312.1:p.Val4448=
XM_024453094.1:c.13344G>A	XP_024308862.1:p.Val4448=
XM_024453095.1:c.13344G>A	XP_024308863.1:p.Val4448=
XM_024453096.1:c.13344G>A	XP_024308864.1:p.Val4448=
XM_024453097.1:c.13344G>A	XP_024308865.1:p.Val4448=
XM_024453098.1:c.13344G>A	XP_024308866.1:p.Val4448=
XM_024453099.1:c.13344G>A	XP_024308867.1:p.Val4448=