Canonical Allele Identifier: CA349610709

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179433466G>T (hg19) ; chr2:g.178568739G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568739G>T , CM000664.2:g.178568739G>T	GRCh38
NC_000002.11:g.179433466G>T , CM000664.1:g.179433466G>T	GRCh37
NC_000002.10:g.179141712G>T	NCBI36
NG_011618.3:g.267064C>A , LRG_391:g.267064C>A
NG_051363.1:g.50913G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.69689C>A (TTN)	ENSP00000343764.6:p.Pro23230Gln
ENST00000342175.11:c.50774C>A (TTN)	ENSP00000340554.6:p.Pro16925Gln
ENST00000359218.10:c.50573C>A (TTN)	ENSP00000352154.5:p.Pro16858Gln
ENST00000342175.10:c.50774C>A (TTN)	ENSP00000340554.6:p.Pro16925Gln
ENST00000342992.10:c.69689C>A (TTN)	ENSP00000343764.6:p.Pro23230Gln
ENST00000359218.9:c.50573C>A (TTN)	ENSP00000352154.5:p.Pro16858Gln
ENST00000460472.6:c.50198C>A (TTN)	ENSP00000434586.1:p.Pro16733Gln
ENST00000589042.5:c.77393C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro25798Gln
ENST00000591111.5:c.72470C>A (TTN)	ENSP00000465570.1:p.Pro24157Gln
ENST00000615779.4:c.72470C>A (TTN)	ENSP00000483597.1:p.Pro24157Gln
NM_001256850.1:c.72470C>A (TTN)	NP_001243779.1:p.Pro24157Gln
NM_001267550.2:c.77393C>A (TTN) MANE Select	NP_001254479.2:p.Pro25798Gln
NM_003319.4:c.50198C>A (TTN)	NP_003310.4:p.Pro16733Gln
NM_133378.4:c.69689C>A (TTN)	NP_596869.4:p.Pro23230Gln
NM_133432.3:c.50573C>A (TTN)	NP_597676.3:p.Pro16858Gln
NM_133437.4:c.50774C>A (TTN)	NP_597681.4:p.Pro16925Gln
NR_038271.1:n.447-2561G>T (TTN-AS1)
NR_038272.1:n.2044-13833G>T (TTN-AS1)
XM_011511729.1:c.76490C>A (TTN)	XP_011510031.1:p.Pro25497Gln
XM_011511730.1:c.50384C>A (TTN)	XP_011510032.1:p.Pro16795Gln
XM_011511731.1:c.50243C>A (TTN)	XP_011510033.1:p.Pro16748Gln
XM_017004819.1:c.76286C>A (TTN)	XP_016860308.1:p.Pro25429Gln
XM_017004820.1:c.71684C>A (TTN)	XP_016860309.1:p.Pro23895Gln
XM_017004821.1:c.71681C>A (TTN)	XP_016860310.1:p.Pro23894Gln
XM_017004822.1:c.68723C>A (TTN)	XP_016860311.1:p.Pro22908Gln
XM_017004823.1:c.50339C>A (TTN)	XP_016860312.1:p.Pro16780Gln
XM_024453094.1:c.71834C>A (TTN)	XP_024308862.1:p.Pro23945Gln
XM_024453095.1:c.71831C>A (TTN)	XP_024308863.1:p.Pro23944Gln
XM_024453096.1:c.71264C>A (TTN)	XP_024308864.1:p.Pro23755Gln
XM_024453097.1:c.68606C>A (TTN)	XP_024308865.1:p.Pro22869Gln
XM_024453098.1:c.68525C>A (TTN)	XP_024308866.1:p.Pro22842Gln
XM_024453099.1:c.50288C>A (TTN)	XP_024308867.1:p.Pro16763Gln
XM_024453100.1:c.40142C>A (TTN)	XP_024308868.1:p.Pro13381Gln