Canonical Allele Identifier: CA349398296

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179391792T>C (hg19) ; chr2:g.178527065T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527065T>C , CM000664.2:g.178527065T>C	GRCh38
NC_000002.11:g.179391792T>C , CM000664.1:g.179391792T>C	GRCh37
NC_000002.10:g.179100038T>C	NCBI36
NG_011618.3:g.308738A>G , LRG_391:g.308738A>G
NG_051363.1:g.9239T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100219A>G (TTN)	ENSP00000343764.6:p.Asn33407Asp
ENST00000342175.11:c.81304A>G (TTN)	ENSP00000340554.6:p.Asn27102Asp
ENST00000359218.10:c.81103A>G (TTN)	ENSP00000352154.5:p.Asn27035Asp
ENST00000342175.10:c.81304A>G (TTN)	ENSP00000340554.6:p.Asn27102Asp
ENST00000342992.10:c.100219A>G (TTN)	ENSP00000343764.6:p.Asn33407Asp
ENST00000359218.9:c.81103A>G (TTN)	ENSP00000352154.5:p.Asn27035Asp
ENST00000460472.6:c.80728A>G (TTN)	ENSP00000434586.1:p.Asn26910Asp
ENST00000589042.5:c.107923A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn35975Asp
ENST00000591111.5:c.103000A>G (TTN)	ENSP00000465570.1:p.Asn34334Asp
ENST00000615779.4:c.103000A>G (TTN)	ENSP00000483597.1:p.Asn34334Asp
NM_001256850.1:c.103000A>G (TTN)	NP_001243779.1:p.Asn34334Asp
NM_001267550.2:c.107923A>G (TTN) MANE Select	NP_001254479.2:p.Asn35975Asp
NM_003319.4:c.80728A>G (TTN)	NP_003310.4:p.Asn26910Asp
NM_133378.4:c.100219A>G (TTN)	NP_596869.4:p.Asn33407Asp
NM_133432.3:c.81103A>G (TTN)	NP_597676.3:p.Asn27035Asp
NM_133437.4:c.81304A>G (TTN)	NP_597681.4:p.Asn27102Asp
NR_038271.1:n.446+3429T>C (TTN-AS1)
NR_038272.1:n.219+3429T>C (TTN-AS1)
XM_011511729.1:c.107020A>G (TTN)	XP_011510031.1:p.Asn35674Asp
XM_011511730.1:c.80914A>G (TTN)	XP_011510032.1:p.Asn26972Asp
XM_011511731.1:c.80773A>G (TTN)	XP_011510033.1:p.Asn26925Asp
XM_017004819.1:c.106816A>G (TTN)	XP_016860308.1:p.Asn35606Asp
XM_017004820.1:c.102214A>G (TTN)	XP_016860309.1:p.Asn34072Asp
XM_017004821.1:c.102211A>G (TTN)	XP_016860310.1:p.Asn34071Asp
XM_017004822.1:c.99253A>G (TTN)	XP_016860311.1:p.Asn33085Asp
XM_017004823.1:c.80869A>G (TTN)	XP_016860312.1:p.Asn26957Asp
XM_024453094.1:c.102364A>G (TTN)	XP_024308862.1:p.Asn34122Asp
XM_024453095.1:c.102361A>G (TTN)	XP_024308863.1:p.Asn34121Asp
XM_024453096.1:c.101794A>G (TTN)	XP_024308864.1:p.Asn33932Asp
XM_024453097.1:c.99136A>G (TTN)	XP_024308865.1:p.Asn33046Asp
XM_024453098.1:c.99055A>G (TTN)	XP_024308866.1:p.Asn33019Asp
XM_024453099.1:c.80818A>G (TTN)	XP_024308867.1:p.Asn26940Asp
XM_024453100.1:c.70672A>G (TTN)	XP_024308868.1:p.Asn23558Asp