Canonical Allele Identifier: CA349620924

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179435173G>C (hg19) ; chr2:g.178570446G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570446G>C , CM000664.2:g.178570446G>C	GRCh38
NC_000002.11:g.179435173G>C , CM000664.1:g.179435173G>C	GRCh37
NC_000002.10:g.179143419G>C	NCBI36
NG_011618.3:g.265357C>G , LRG_391:g.265357C>G
NG_051363.1:g.52620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.67982C>G (TTN)	ENSP00000343764.6:p.Pro22661Arg
ENST00000342175.11:c.49067C>G (TTN)	ENSP00000340554.6:p.Pro16356Arg
ENST00000359218.10:c.48866C>G (TTN)	ENSP00000352154.5:p.Pro16289Arg
ENST00000342175.10:c.49067C>G (TTN)	ENSP00000340554.6:p.Pro16356Arg
ENST00000342992.10:c.67982C>G (TTN)	ENSP00000343764.6:p.Pro22661Arg
ENST00000359218.9:c.48866C>G (TTN)	ENSP00000352154.5:p.Pro16289Arg
ENST00000460472.6:c.48491C>G (TTN)	ENSP00000434586.1:p.Pro16164Arg
ENST00000589042.5:c.75686C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro25229Arg
ENST00000591111.5:c.70763C>G (TTN)	ENSP00000465570.1:p.Pro23588Arg
ENST00000615779.4:c.70763C>G (TTN)	ENSP00000483597.1:p.Pro23588Arg
NM_001256850.1:c.70763C>G (TTN)	NP_001243779.1:p.Pro23588Arg
NM_001267550.2:c.75686C>G (TTN) MANE Select	NP_001254479.2:p.Pro25229Arg
NM_003319.4:c.48491C>G (TTN)	NP_003310.4:p.Pro16164Arg
NM_133378.4:c.67982C>G (TTN)	NP_596869.4:p.Pro22661Arg
NM_133432.3:c.48866C>G (TTN)	NP_597676.3:p.Pro16289Arg
NM_133437.4:c.49067C>G (TTN)	NP_597681.4:p.Pro16356Arg
NR_038271.1:n.447-854G>C (TTN-AS1)
NR_038272.1:n.2044-12126G>C (TTN-AS1)
XM_011511729.1:c.74783C>G (TTN)	XP_011510031.1:p.Pro24928Arg
XM_011511730.1:c.48677C>G (TTN)	XP_011510032.1:p.Pro16226Arg
XM_011511731.1:c.48536C>G (TTN)	XP_011510033.1:p.Pro16179Arg
XM_017004819.1:c.74579C>G (TTN)	XP_016860308.1:p.Pro24860Arg
XM_017004820.1:c.69977C>G (TTN)	XP_016860309.1:p.Pro23326Arg
XM_017004821.1:c.69974C>G (TTN)	XP_016860310.1:p.Pro23325Arg
XM_017004822.1:c.67016C>G (TTN)	XP_016860311.1:p.Pro22339Arg
XM_017004823.1:c.48632C>G (TTN)	XP_016860312.1:p.Pro16211Arg
XM_024453094.1:c.70127C>G (TTN)	XP_024308862.1:p.Pro23376Arg
XM_024453095.1:c.70124C>G (TTN)	XP_024308863.1:p.Pro23375Arg
XM_024453096.1:c.69557C>G (TTN)	XP_024308864.1:p.Pro23186Arg
XM_024453097.1:c.66899C>G (TTN)	XP_024308865.1:p.Pro22300Arg
XM_024453098.1:c.66818C>G (TTN)	XP_024308866.1:p.Pro22273Arg
XM_024453099.1:c.48581C>G (TTN)	XP_024308867.1:p.Pro16194Arg
XM_024453100.1:c.38435C>G (TTN)	XP_024308868.1:p.Pro12812Arg