Canonical Allele Identifier: CA349652112

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179497704G>A (hg19) ; chr2:g.178632977G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178632977G>A , CM000664.2:g.178632977G>A	GRCh38
NC_000002.11:g.179497704G>A , CM000664.1:g.179497704G>A	GRCh37
NC_000002.10:g.179205949G>A	NCBI36
NG_011618.3:g.202826C>T , LRG_391:g.202826C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.35450C>T	ENSP00000343764.6:p.Thr11817Ile
ENST00000342175.11:c.16535C>T	ENSP00000340554.6:p.Thr5512Ile
ENST00000359218.10:c.16334C>T	ENSP00000352154.5:p.Thr5445Ile
ENST00000342175.10:c.16535C>T	ENSP00000340554.6:p.Thr5512Ile
ENST00000342992.10:c.35450C>T	ENSP00000343764.6:p.Thr11817Ile
ENST00000359218.9:c.16334C>T	ENSP00000352154.5:p.Thr5445Ile
ENST00000460472.6:c.15959C>T	ENSP00000434586.1:p.Thr5320Ile
ENST00000589042.5:c.43154C>T MANE Select	ENSP00000467141.1:p.Thr14385Ile
ENST00000591111.5:c.38231C>T	ENSP00000465570.1:p.Thr12744Ile
ENST00000615779.4:c.38231C>T	ENSP00000483597.1:p.Thr12744Ile
NM_001256850.1:c.38231C>T	NP_001243779.1:p.Thr12744Ile
NM_001267550.2:c.43154C>T MANE Select	NP_001254479.2:p.Thr14385Ile
NM_003319.4:c.15959C>T	NP_003310.4:p.Thr5320Ile
NM_133378.4:c.35450C>T	NP_596869.4:p.Thr11817Ile
NM_133432.3:c.16334C>T	NP_597676.3:p.Thr5445Ile
NM_133437.4:c.16535C>T	NP_597681.4:p.Thr5512Ile
XM_011511729.1:c.42251C>T	XP_011510031.1:p.Thr14084Ile
XM_011511730.1:c.16145C>T	XP_011510032.1:p.Thr5382Ile
XM_011511731.1:c.16004C>T	XP_011510033.1:p.Thr5335Ile
XM_017004819.1:c.42047C>T	XP_016860308.1:p.Thr14016Ile
XM_017004820.1:c.37445C>T	XP_016860309.1:p.Thr12482Ile
XM_017004821.1:c.37442C>T	XP_016860310.1:p.Thr12481Ile
XM_017004822.1:c.34484C>T	XP_016860311.1:p.Thr11495Ile
XM_017004823.1:c.16100C>T	XP_016860312.1:p.Thr5367Ile
XM_024453094.1:c.37595C>T	XP_024308862.1:p.Thr12532Ile
XM_024453095.1:c.37592C>T	XP_024308863.1:p.Thr12531Ile
XM_024453096.1:c.37025C>T	XP_024308864.1:p.Thr12342Ile
XM_024453097.1:c.34367C>T	XP_024308865.1:p.Thr11456Ile
XM_024453098.1:c.34286C>T	XP_024308866.1:p.Thr11429Ile
XM_024453099.1:c.16049C>T	XP_024308867.1:p.Thr5350Ile
XM_024453100.1:c.5903C>T	XP_024308868.1:p.Thr1968Ile