Canonical Allele Identifier: CA349661756

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501437G>A (hg19) ; chr2:g.178636710G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636710G>A , CM000664.2:g.178636710G>A	GRCh38
NC_000002.11:g.179501437G>A , CM000664.1:g.179501437G>A	GRCh37
NC_000002.10:g.179209682G>A	NCBI36
NG_011618.3:g.199093C>T , LRG_391:g.199093C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33313C>T	ENSP00000343764.6:p.Pro11105Ser
ENST00000342175.11:c.14398C>T	ENSP00000340554.6:p.Pro4800Ser
ENST00000359218.10:c.14197C>T	ENSP00000352154.5:p.Pro4733Ser
ENST00000342175.10:c.14398C>T	ENSP00000340554.6:p.Pro4800Ser
ENST00000342992.10:c.33313C>T	ENSP00000343764.6:p.Pro11105Ser
ENST00000359218.9:c.14197C>T	ENSP00000352154.5:p.Pro4733Ser
ENST00000460472.6:c.13822C>T	ENSP00000434586.1:p.Pro4608Ser
ENST00000589042.5:c.41017C>T MANE Select	ENSP00000467141.1:p.Pro13673Ser
ENST00000591111.5:c.36094C>T	ENSP00000465570.1:p.Pro12032Ser
ENST00000615779.4:c.36094C>T	ENSP00000483597.1:p.Pro12032Ser
NM_001256850.1:c.36094C>T	NP_001243779.1:p.Pro12032Ser
NM_001267550.2:c.41017C>T MANE Select	NP_001254479.2:p.Pro13673Ser
NM_003319.4:c.13822C>T	NP_003310.4:p.Pro4608Ser
NM_133378.4:c.33313C>T	NP_596869.4:p.Pro11105Ser
NM_133432.3:c.14197C>T	NP_597676.3:p.Pro4733Ser
NM_133437.4:c.14398C>T	NP_597681.4:p.Pro4800Ser
XM_011511729.1:c.40114C>T	XP_011510031.1:p.Pro13372Ser
XM_011511730.1:c.14008C>T	XP_011510032.1:p.Pro4670Ser
XM_011511731.1:c.13867C>T	XP_011510033.1:p.Pro4623Ser
XM_017004819.1:c.39910C>T	XP_016860308.1:p.Pro13304Ser
XM_017004820.1:c.35308C>T	XP_016860309.1:p.Pro11770Ser
XM_017004821.1:c.35305C>T	XP_016860310.1:p.Pro11769Ser
XM_017004822.1:c.32347C>T	XP_016860311.1:p.Pro10783Ser
XM_017004823.1:c.13963C>T	XP_016860312.1:p.Pro4655Ser
XM_024453094.1:c.35458C>T	XP_024308862.1:p.Pro11820Ser
XM_024453095.1:c.35455C>T	XP_024308863.1:p.Pro11819Ser
XM_024453096.1:c.34888C>T	XP_024308864.1:p.Pro11630Ser
XM_024453097.1:c.32230C>T	XP_024308865.1:p.Pro10744Ser
XM_024453098.1:c.32149C>T	XP_024308866.1:p.Pro10717Ser
XM_024453099.1:c.13912C>T	XP_024308867.1:p.Pro4638Ser
XM_024453100.1:c.3766C>T	XP_024308868.1:p.Pro1256Ser