Canonical Allele Identifier: CA349495663

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414512T>G (hg19) ; chr2:g.178549785T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549785T>G , CM000664.2:g.178549785T>G	GRCh38
NC_000002.11:g.179414512T>G , CM000664.1:g.179414512T>G	GRCh37
NC_000002.10:g.179122758T>G	NCBI36
NG_011618.3:g.286018A>C , LRG_391:g.286018A>C
NG_051363.1:g.31959T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84233A>C (TTN)	ENSP00000343764.6:p.Asn28078Thr
ENST00000342175.11:c.65318A>C (TTN)	ENSP00000340554.6:p.Asn21773Thr
ENST00000359218.10:c.65117A>C (TTN)	ENSP00000352154.5:p.Asn21706Thr
ENST00000342175.10:c.65318A>C (TTN)	ENSP00000340554.6:p.Asn21773Thr
ENST00000342992.10:c.84233A>C (TTN)	ENSP00000343764.6:p.Asn28078Thr
ENST00000359218.9:c.65117A>C (TTN)	ENSP00000352154.5:p.Asn21706Thr
ENST00000460472.6:c.64742A>C (TTN)	ENSP00000434586.1:p.Asn21581Thr
ENST00000589042.5:c.91937A>C (TTN) MANE Select	ENSP00000467141.1:p.Asn30646Thr
ENST00000591111.5:c.87014A>C (TTN)	ENSP00000465570.1:p.Asn29005Thr
ENST00000615779.4:c.87014A>C (TTN)	ENSP00000483597.1:p.Asn29005Thr
NM_001256850.1:c.87014A>C (TTN)	NP_001243779.1:p.Asn29005Thr
NM_001267550.2:c.91937A>C (TTN) MANE Select	NP_001254479.2:p.Asn30646Thr
NM_003319.4:c.64742A>C (TTN)	NP_003310.4:p.Asn21581Thr
NM_133378.4:c.84233A>C (TTN)	NP_596869.4:p.Asn28078Thr
NM_133432.3:c.65117A>C (TTN)	NP_597676.3:p.Asn21706Thr
NM_133437.4:c.65318A>C (TTN)	NP_597681.4:p.Asn21773Thr
NR_038271.1:n.447-21515T>G (TTN-AS1)
NR_038272.1:n.2043+7424T>G (TTN-AS1)
XM_011511729.1:c.91034A>C (TTN)	XP_011510031.1:p.Asn30345Thr
XM_011511730.1:c.64928A>C (TTN)	XP_011510032.1:p.Asn21643Thr
XM_011511731.1:c.64787A>C (TTN)	XP_011510033.1:p.Asn21596Thr
XM_017004819.1:c.90830A>C (TTN)	XP_016860308.1:p.Asn30277Thr
XM_017004820.1:c.86228A>C (TTN)	XP_016860309.1:p.Asn28743Thr
XM_017004821.1:c.86225A>C (TTN)	XP_016860310.1:p.Asn28742Thr
XM_017004822.1:c.83267A>C (TTN)	XP_016860311.1:p.Asn27756Thr
XM_017004823.1:c.64883A>C (TTN)	XP_016860312.1:p.Asn21628Thr
XM_024453094.1:c.86378A>C (TTN)	XP_024308862.1:p.Asn28793Thr
XM_024453095.1:c.86375A>C (TTN)	XP_024308863.1:p.Asn28792Thr
XM_024453096.1:c.85808A>C (TTN)	XP_024308864.1:p.Asn28603Thr
XM_024453097.1:c.83150A>C (TTN)	XP_024308865.1:p.Asn27717Thr
XM_024453098.1:c.83069A>C (TTN)	XP_024308866.1:p.Asn27690Thr
XM_024453099.1:c.64832A>C (TTN)	XP_024308867.1:p.Asn21611Thr
XM_024453100.1:c.54686A>C (TTN)	XP_024308868.1:p.Asn18229Thr