Canonical Allele Identifier: CA200064

Gene: TTN TTN-AS1

Linked Data

• ClinVar Variation Id: 192200
• ClinVar RCV Id: RCV000172785
• dbSNP Id: rs786205328
• MyVariant Identifiers: chr2:g.179414513T>C (hg19) ; chr2:g.178549786T>C (hg38)
• PubMed: PMID:23861362

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549786T>C , CM000664.2:g.178549786T>C	GRCh38
NC_000002.11:g.179414513T>C , CM000664.1:g.179414513T>C	GRCh37
NC_000002.10:g.179122759T>C	NCBI36
NG_011618.3:g.286017A>G , LRG_391:g.286017A>G
NG_051363.1:g.31960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84232A>G (TTN)	ENSP00000343764.6:p.Asn28078Asp
ENST00000342175.11:c.65317A>G (TTN)	ENSP00000340554.6:p.Asn21773Asp
ENST00000359218.10:c.65116A>G (TTN)	ENSP00000352154.5:p.Asn21706Asp
ENST00000342175.10:c.65317A>G (TTN)	ENSP00000340554.6:p.Asn21773Asp
ENST00000342992.10:c.84232A>G (TTN)	ENSP00000343764.6:p.Asn28078Asp
ENST00000359218.9:c.65116A>G (TTN)	ENSP00000352154.5:p.Asn21706Asp
ENST00000460472.6:c.64741A>G (TTN)	ENSP00000434586.1:p.Asn21581Asp
ENST00000589042.5:c.91936A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn30646Asp
ENST00000591111.5:c.87013A>G (TTN)	ENSP00000465570.1:p.Asn29005Asp
ENST00000615779.4:c.87013A>G (TTN)	ENSP00000483597.1:p.Asn29005Asp
NM_001256850.1:c.87013A>G (TTN)	NP_001243779.1:p.Asn29005Asp
NM_001267550.2:c.91936A>G (TTN) MANE Select	NP_001254479.2:p.Asn30646Asp
NM_003319.4:c.64741A>G (TTN)	NP_003310.4:p.Asn21581Asp
NM_133378.4:c.84232A>G (TTN)	NP_596869.4:p.Asn28078Asp
NM_133432.3:c.65116A>G (TTN)	NP_597676.3:p.Asn21706Asp
NM_133437.4:c.65317A>G (TTN)	NP_597681.4:p.Asn21773Asp
NR_038271.1:n.447-21514T>C (TTN-AS1)
NR_038272.1:n.2043+7425T>C (TTN-AS1)
XM_011511729.1:c.91033A>G (TTN)	XP_011510031.1:p.Asn30345Asp
XM_011511730.1:c.64927A>G (TTN)	XP_011510032.1:p.Asn21643Asp
XM_011511731.1:c.64786A>G (TTN)	XP_011510033.1:p.Asn21596Asp
XM_017004819.1:c.90829A>G (TTN)	XP_016860308.1:p.Asn30277Asp
XM_017004820.1:c.86227A>G (TTN)	XP_016860309.1:p.Asn28743Asp
XM_017004821.1:c.86224A>G (TTN)	XP_016860310.1:p.Asn28742Asp
XM_017004822.1:c.83266A>G (TTN)	XP_016860311.1:p.Asn27756Asp
XM_017004823.1:c.64882A>G (TTN)	XP_016860312.1:p.Asn21628Asp
XM_024453094.1:c.86377A>G (TTN)	XP_024308862.1:p.Asn28793Asp
XM_024453095.1:c.86374A>G (TTN)	XP_024308863.1:p.Asn28792Asp
XM_024453096.1:c.85807A>G (TTN)	XP_024308864.1:p.Asn28603Asp
XM_024453097.1:c.83149A>G (TTN)	XP_024308865.1:p.Asn27717Asp
XM_024453098.1:c.83068A>G (TTN)	XP_024308866.1:p.Asn27690Asp
XM_024453099.1:c.64831A>G (TTN)	XP_024308867.1:p.Asn21611Asp
XM_024453100.1:c.54685A>G (TTN)	XP_024308868.1:p.Asn18229Asp