Canonical Allele Identifier: CA349411536

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396842A>C (hg19) ; chr2:g.178532115A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532115A>C , CM000664.2:g.178532115A>C	GRCh38
NC_000002.11:g.179396842A>C , CM000664.1:g.179396842A>C	GRCh37
NC_000002.10:g.179105088A>C	NCBI36
NG_011618.3:g.303688T>G , LRG_391:g.303688T>G
NG_051363.1:g.14289A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96796T>G (TTN)	ENSP00000343764.6:p.Ser32266Ala
ENST00000342175.11:c.77881T>G (TTN)	ENSP00000340554.6:p.Ser25961Ala
ENST00000359218.10:c.77680T>G (TTN)	ENSP00000352154.5:p.Ser25894Ala
ENST00000342175.10:c.77881T>G (TTN)	ENSP00000340554.6:p.Ser25961Ala
ENST00000342992.10:c.96796T>G (TTN)	ENSP00000343764.6:p.Ser32266Ala
ENST00000359218.9:c.77680T>G (TTN)	ENSP00000352154.5:p.Ser25894Ala
ENST00000460472.6:c.77305T>G (TTN)	ENSP00000434586.1:p.Ser25769Ala
ENST00000589042.5:c.104500T>G (TTN) MANE Select	ENSP00000467141.1:p.Ser34834Ala
ENST00000591111.5:c.99577T>G (TTN)	ENSP00000465570.1:p.Ser33193Ala
ENST00000615779.4:c.99577T>G (TTN)	ENSP00000483597.1:p.Ser33193Ala
NM_001256850.1:c.99577T>G (TTN)	NP_001243779.1:p.Ser33193Ala
NM_001267550.2:c.104500T>G (TTN) MANE Select	NP_001254479.2:p.Ser34834Ala
NM_003319.4:c.77305T>G (TTN)	NP_003310.4:p.Ser25769Ala
NM_133378.4:c.96796T>G (TTN)	NP_596869.4:p.Ser32266Ala
NM_133432.3:c.77680T>G (TTN)	NP_597676.3:p.Ser25894Ala
NM_133437.4:c.77881T>G (TTN)	NP_597681.4:p.Ser25961Ala
NR_038271.1:n.446+8479A>C (TTN-AS1)
NR_038272.1:n.220-3617A>C (TTN-AS1)
XM_011511729.1:c.103597T>G (TTN)	XP_011510031.1:p.Ser34533Ala
XM_011511730.1:c.77491T>G (TTN)	XP_011510032.1:p.Ser25831Ala
XM_011511731.1:c.77350T>G (TTN)	XP_011510033.1:p.Ser25784Ala
XM_017004819.1:c.103393T>G (TTN)	XP_016860308.1:p.Ser34465Ala
XM_017004820.1:c.98791T>G (TTN)	XP_016860309.1:p.Ser32931Ala
XM_017004821.1:c.98788T>G (TTN)	XP_016860310.1:p.Ser32930Ala
XM_017004822.1:c.95830T>G (TTN)	XP_016860311.1:p.Ser31944Ala
XM_017004823.1:c.77446T>G (TTN)	XP_016860312.1:p.Ser25816Ala
XM_024453094.1:c.98941T>G (TTN)	XP_024308862.1:p.Ser32981Ala
XM_024453095.1:c.98938T>G (TTN)	XP_024308863.1:p.Ser32980Ala
XM_024453096.1:c.98371T>G (TTN)	XP_024308864.1:p.Ser32791Ala
XM_024453097.1:c.95713T>G (TTN)	XP_024308865.1:p.Ser31905Ala
XM_024453098.1:c.95632T>G (TTN)	XP_024308866.1:p.Ser31878Ala
XM_024453099.1:c.77395T>G (TTN)	XP_024308867.1:p.Ser25799Ala
XM_024453100.1:c.67249T>G (TTN)	XP_024308868.1:p.Ser22417Ala