Canonical Allele Identifier: CA349406370

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395071G>T (hg19) ; chr2:g.178530344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530344G>T , CM000664.2:g.178530344G>T	GRCh38
NC_000002.11:g.179395071G>T , CM000664.1:g.179395071G>T	GRCh37
NC_000002.10:g.179103317G>T	NCBI36
NG_011618.3:g.305459C>A , LRG_391:g.305459C>A
NG_051363.1:g.12518G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98567C>A (TTN)	ENSP00000343764.6:p.Thr32856Asn
ENST00000342175.11:c.79652C>A (TTN)	ENSP00000340554.6:p.Thr26551Asn
ENST00000359218.10:c.79451C>A (TTN)	ENSP00000352154.5:p.Thr26484Asn
ENST00000342175.10:c.79652C>A (TTN)	ENSP00000340554.6:p.Thr26551Asn
ENST00000342992.10:c.98567C>A (TTN)	ENSP00000343764.6:p.Thr32856Asn
ENST00000359218.9:c.79451C>A (TTN)	ENSP00000352154.5:p.Thr26484Asn
ENST00000460472.6:c.79076C>A (TTN)	ENSP00000434586.1:p.Thr26359Asn
ENST00000589042.5:c.106271C>A (TTN) MANE Select	ENSP00000467141.1:p.Thr35424Asn
ENST00000591111.5:c.101348C>A (TTN)	ENSP00000465570.1:p.Thr33783Asn
ENST00000615779.4:c.101348C>A (TTN)	ENSP00000483597.1:p.Thr33783Asn
NM_001256850.1:c.101348C>A (TTN)	NP_001243779.1:p.Thr33783Asn
NM_001267550.2:c.106271C>A (TTN) MANE Select	NP_001254479.2:p.Thr35424Asn
NM_003319.4:c.79076C>A (TTN)	NP_003310.4:p.Thr26359Asn
NM_133378.4:c.98567C>A (TTN)	NP_596869.4:p.Thr32856Asn
NM_133432.3:c.79451C>A (TTN)	NP_597676.3:p.Thr26484Asn
NM_133437.4:c.79652C>A (TTN)	NP_597681.4:p.Thr26551Asn
NR_038271.1:n.446+6708G>T (TTN-AS1)
NR_038272.1:n.220-5388G>T (TTN-AS1)
XM_011511729.1:c.105368C>A (TTN)	XP_011510031.1:p.Thr35123Asn
XM_011511730.1:c.79262C>A (TTN)	XP_011510032.1:p.Thr26421Asn
XM_011511731.1:c.79121C>A (TTN)	XP_011510033.1:p.Thr26374Asn
XM_017004819.1:c.105164C>A (TTN)	XP_016860308.1:p.Thr35055Asn
XM_017004820.1:c.100562C>A (TTN)	XP_016860309.1:p.Thr33521Asn
XM_017004821.1:c.100559C>A (TTN)	XP_016860310.1:p.Thr33520Asn
XM_017004822.1:c.97601C>A (TTN)	XP_016860311.1:p.Thr32534Asn
XM_017004823.1:c.79217C>A (TTN)	XP_016860312.1:p.Thr26406Asn
XM_024453094.1:c.100712C>A (TTN)	XP_024308862.1:p.Thr33571Asn
XM_024453095.1:c.100709C>A (TTN)	XP_024308863.1:p.Thr33570Asn
XM_024453096.1:c.100142C>A (TTN)	XP_024308864.1:p.Thr33381Asn
XM_024453097.1:c.97484C>A (TTN)	XP_024308865.1:p.Thr32495Asn
XM_024453098.1:c.97403C>A (TTN)	XP_024308866.1:p.Thr32468Asn
XM_024453099.1:c.79166C>A (TTN)	XP_024308867.1:p.Thr26389Asn
XM_024453100.1:c.69020C>A (TTN)	XP_024308868.1:p.Thr23007Asn