Canonical Allele Identifier: CA349435969

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179449299G>A (hg19) ; chr2:g.178584572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584572G>A , CM000664.2:g.178584572G>A	GRCh38
NC_000002.11:g.179449299G>A , CM000664.1:g.179449299G>A	GRCh37
NC_000002.10:g.179157545G>A	NCBI36
NG_011618.3:g.251231C>T , LRG_391:g.251231C>T
NG_051363.1:g.66746G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57275C>T (TTN)	ENSP00000343764.6:p.Pro19092Leu
ENST00000342175.11:c.38360C>T (TTN)	ENSP00000340554.6:p.Pro12787Leu
ENST00000359218.10:c.38159C>T (TTN)	ENSP00000352154.5:p.Pro12720Leu
ENST00000342175.10:c.38360C>T (TTN)	ENSP00000340554.6:p.Pro12787Leu
ENST00000342992.10:c.57275C>T (TTN)	ENSP00000343764.6:p.Pro19092Leu
ENST00000359218.9:c.38159C>T (TTN)	ENSP00000352154.5:p.Pro12720Leu
ENST00000460472.6:c.37784C>T (TTN)	ENSP00000434586.1:p.Pro12595Leu
ENST00000589042.5:c.64979C>T (TTN) MANE Select	ENSP00000467141.1:p.Pro21660Leu
ENST00000591111.5:c.60056C>T (TTN)	ENSP00000465570.1:p.Pro20019Leu
ENST00000615779.4:c.60056C>T (TTN)	ENSP00000483597.1:p.Pro20019Leu
NM_001256850.1:c.60056C>T (TTN)	NP_001243779.1:p.Pro20019Leu
NM_001267550.2:c.64979C>T (TTN) MANE Select	NP_001254479.2:p.Pro21660Leu
NM_003319.4:c.37784C>T (TTN)	NP_003310.4:p.Pro12595Leu
NM_133378.4:c.57275C>T (TTN)	NP_596869.4:p.Pro19092Leu
NM_133432.3:c.38159C>T (TTN)	NP_597676.3:p.Pro12720Leu
NM_133437.4:c.38360C>T (TTN)	NP_597681.4:p.Pro12787Leu
NR_038271.1:n.597-13024G>A (TTN-AS1)
NR_038272.1:n.2768-1G>A (TTN-AS1)
XM_011511729.1:c.64076C>T (TTN)	XP_011510031.1:p.Pro21359Leu
XM_011511730.1:c.37970C>T (TTN)	XP_011510032.1:p.Pro12657Leu
XM_011511731.1:c.37829C>T (TTN)	XP_011510033.1:p.Pro12610Leu
XM_017004819.1:c.63872C>T (TTN)	XP_016860308.1:p.Pro21291Leu
XM_017004820.1:c.59270C>T (TTN)	XP_016860309.1:p.Pro19757Leu
XM_017004821.1:c.59267C>T (TTN)	XP_016860310.1:p.Pro19756Leu
XM_017004822.1:c.56309C>T (TTN)	XP_016860311.1:p.Pro18770Leu
XM_017004823.1:c.37925C>T (TTN)	XP_016860312.1:p.Pro12642Leu
XM_024453094.1:c.59420C>T (TTN)	XP_024308862.1:p.Pro19807Leu
XM_024453095.1:c.59417C>T (TTN)	XP_024308863.1:p.Pro19806Leu
XM_024453096.1:c.58850C>T (TTN)	XP_024308864.1:p.Pro19617Leu
XM_024453097.1:c.56192C>T (TTN)	XP_024308865.1:p.Pro18731Leu
XM_024453098.1:c.56111C>T (TTN)	XP_024308866.1:p.Pro18704Leu
XM_024453099.1:c.37874C>T (TTN)	XP_024308867.1:p.Pro12625Leu
XM_024453100.1:c.27728C>T (TTN)	XP_024308868.1:p.Pro9243Leu