Canonical Allele Identifier: CA349411825

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396947A>G (hg19) ; chr2:g.178532220A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532220A>G , CM000664.2:g.178532220A>G	GRCh38
NC_000002.11:g.179396947A>G , CM000664.1:g.179396947A>G	GRCh37
NC_000002.10:g.179105193A>G	NCBI36
NG_011618.3:g.303583T>C , LRG_391:g.303583T>C
NG_051363.1:g.14394A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96691T>C (TTN)	ENSP00000343764.6:p.Ser32231Pro
ENST00000342175.11:c.77776T>C (TTN)	ENSP00000340554.6:p.Ser25926Pro
ENST00000359218.10:c.77575T>C (TTN)	ENSP00000352154.5:p.Ser25859Pro
ENST00000342175.10:c.77776T>C (TTN)	ENSP00000340554.6:p.Ser25926Pro
ENST00000342992.10:c.96691T>C (TTN)	ENSP00000343764.6:p.Ser32231Pro
ENST00000359218.9:c.77575T>C (TTN)	ENSP00000352154.5:p.Ser25859Pro
ENST00000460472.6:c.77200T>C (TTN)	ENSP00000434586.1:p.Ser25734Pro
ENST00000589042.5:c.104395T>C (TTN) MANE Select	ENSP00000467141.1:p.Ser34799Pro
ENST00000591111.5:c.99472T>C (TTN)	ENSP00000465570.1:p.Ser33158Pro
ENST00000615779.4:c.99472T>C (TTN)	ENSP00000483597.1:p.Ser33158Pro
NM_001256850.1:c.99472T>C (TTN)	NP_001243779.1:p.Ser33158Pro
NM_001267550.2:c.104395T>C (TTN) MANE Select	NP_001254479.2:p.Ser34799Pro
NM_003319.4:c.77200T>C (TTN)	NP_003310.4:p.Ser25734Pro
NM_133378.4:c.96691T>C (TTN)	NP_596869.4:p.Ser32231Pro
NM_133432.3:c.77575T>C (TTN)	NP_597676.3:p.Ser25859Pro
NM_133437.4:c.77776T>C (TTN)	NP_597681.4:p.Ser25926Pro
NR_038271.1:n.446+8584A>G (TTN-AS1)
NR_038272.1:n.220-3512A>G (TTN-AS1)
XM_011511729.1:c.103492T>C (TTN)	XP_011510031.1:p.Ser34498Pro
XM_011511730.1:c.77386T>C (TTN)	XP_011510032.1:p.Ser25796Pro
XM_011511731.1:c.77245T>C (TTN)	XP_011510033.1:p.Ser25749Pro
XM_017004819.1:c.103288T>C (TTN)	XP_016860308.1:p.Ser34430Pro
XM_017004820.1:c.98686T>C (TTN)	XP_016860309.1:p.Ser32896Pro
XM_017004821.1:c.98683T>C (TTN)	XP_016860310.1:p.Ser32895Pro
XM_017004822.1:c.95725T>C (TTN)	XP_016860311.1:p.Ser31909Pro
XM_017004823.1:c.77341T>C (TTN)	XP_016860312.1:p.Ser25781Pro
XM_024453094.1:c.98836T>C (TTN)	XP_024308862.1:p.Ser32946Pro
XM_024453095.1:c.98833T>C (TTN)	XP_024308863.1:p.Ser32945Pro
XM_024453096.1:c.98266T>C (TTN)	XP_024308864.1:p.Ser32756Pro
XM_024453097.1:c.95608T>C (TTN)	XP_024308865.1:p.Ser31870Pro
XM_024453098.1:c.95527T>C (TTN)	XP_024308866.1:p.Ser31843Pro
XM_024453099.1:c.77290T>C (TTN)	XP_024308867.1:p.Ser25764Pro
XM_024453100.1:c.67144T>C (TTN)	XP_024308868.1:p.Ser22382Pro