Canonical Allele Identifier: CA349470169

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179411348C>G (hg19) ; chr2:g.178546621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546621C>G , CM000664.2:g.178546621C>G	GRCh38
NC_000002.11:g.179411348C>G , CM000664.1:g.179411348C>G	GRCh37
NC_000002.10:g.179119594C>G	NCBI36
NG_011618.3:g.289182G>C , LRG_391:g.289182G>C
NG_051363.1:g.28795C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.87103G>C (TTN)	ENSP00000343764.6:p.Val29035Leu
ENST00000342175.11:c.68188G>C (TTN)	ENSP00000340554.6:p.Val22730Leu
ENST00000359218.10:c.67987G>C (TTN)	ENSP00000352154.5:p.Val22663Leu
ENST00000342175.10:c.68188G>C (TTN)	ENSP00000340554.6:p.Val22730Leu
ENST00000342992.10:c.87103G>C (TTN)	ENSP00000343764.6:p.Val29035Leu
ENST00000359218.9:c.67987G>C (TTN)	ENSP00000352154.5:p.Val22663Leu
ENST00000460472.6:c.67612G>C (TTN)	ENSP00000434586.1:p.Val22538Leu
ENST00000589042.5:c.94807G>C (TTN) MANE Select	ENSP00000467141.1:p.Val31603Leu
ENST00000591111.5:c.89884G>C (TTN)	ENSP00000465570.1:p.Val29962Leu
ENST00000615779.4:c.89884G>C (TTN)	ENSP00000483597.1:p.Val29962Leu
NM_001256850.1:c.89884G>C (TTN)	NP_001243779.1:p.Val29962Leu
NM_001267550.2:c.94807G>C (TTN) MANE Select	NP_001254479.2:p.Val31603Leu
NM_003319.4:c.67612G>C (TTN)	NP_003310.4:p.Val22538Leu
NM_133378.4:c.87103G>C (TTN)	NP_596869.4:p.Val29035Leu
NM_133432.3:c.67987G>C (TTN)	NP_597676.3:p.Val22663Leu
NM_133437.4:c.68188G>C (TTN)	NP_597681.4:p.Val22730Leu
NR_038271.1:n.446+22985C>G (TTN-AS1)
NR_038272.1:n.2043+4260C>G (TTN-AS1)
XM_011511729.1:c.93904G>C (TTN)	XP_011510031.1:p.Val31302Leu
XM_011511730.1:c.67798G>C (TTN)	XP_011510032.1:p.Val22600Leu
XM_011511731.1:c.67657G>C (TTN)	XP_011510033.1:p.Val22553Leu
XM_017004819.1:c.93700G>C (TTN)	XP_016860308.1:p.Val31234Leu
XM_017004820.1:c.89098G>C (TTN)	XP_016860309.1:p.Val29700Leu
XM_017004821.1:c.89095G>C (TTN)	XP_016860310.1:p.Val29699Leu
XM_017004822.1:c.86137G>C (TTN)	XP_016860311.1:p.Val28713Leu
XM_017004823.1:c.67753G>C (TTN)	XP_016860312.1:p.Val22585Leu
XM_024453094.1:c.89248G>C (TTN)	XP_024308862.1:p.Val29750Leu
XM_024453095.1:c.89245G>C (TTN)	XP_024308863.1:p.Val29749Leu
XM_024453096.1:c.88678G>C (TTN)	XP_024308864.1:p.Val29560Leu
XM_024453097.1:c.86020G>C (TTN)	XP_024308865.1:p.Val28674Leu
XM_024453098.1:c.85939G>C (TTN)	XP_024308866.1:p.Val28647Leu
XM_024453099.1:c.67702G>C (TTN)	XP_024308867.1:p.Val22568Leu
XM_024453100.1:c.57556G>C (TTN)	XP_024308868.1:p.Val19186Leu