Canonical Allele Identifier: CA349411894

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396975T>G (hg19) ; chr2:g.178532248T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532248T>G , CM000664.2:g.178532248T>G	GRCh38
NC_000002.11:g.179396975T>G , CM000664.1:g.179396975T>G	GRCh37
NC_000002.10:g.179105221T>G	NCBI36
NG_011618.3:g.303555A>C , LRG_391:g.303555A>C
NG_051363.1:g.14422T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96663A>C (TTN)	ENSP00000343764.6:p.Glu32221Asp
ENST00000342175.11:c.77748A>C (TTN)	ENSP00000340554.6:p.Glu25916Asp
ENST00000359218.10:c.77547A>C (TTN)	ENSP00000352154.5:p.Glu25849Asp
ENST00000342175.10:c.77748A>C (TTN)	ENSP00000340554.6:p.Glu25916Asp
ENST00000342992.10:c.96663A>C (TTN)	ENSP00000343764.6:p.Glu32221Asp
ENST00000359218.9:c.77547A>C (TTN)	ENSP00000352154.5:p.Glu25849Asp
ENST00000460472.6:c.77172A>C (TTN)	ENSP00000434586.1:p.Glu25724Asp
ENST00000589042.5:c.104367A>C (TTN) MANE Select	ENSP00000467141.1:p.Glu34789Asp
ENST00000591111.5:c.99444A>C (TTN)	ENSP00000465570.1:p.Glu33148Asp
ENST00000615779.4:c.99444A>C (TTN)	ENSP00000483597.1:p.Glu33148Asp
NM_001256850.1:c.99444A>C (TTN)	NP_001243779.1:p.Glu33148Asp
NM_001267550.2:c.104367A>C (TTN) MANE Select	NP_001254479.2:p.Glu34789Asp
NM_003319.4:c.77172A>C (TTN)	NP_003310.4:p.Glu25724Asp
NM_133378.4:c.96663A>C (TTN)	NP_596869.4:p.Glu32221Asp
NM_133432.3:c.77547A>C (TTN)	NP_597676.3:p.Glu25849Asp
NM_133437.4:c.77748A>C (TTN)	NP_597681.4:p.Glu25916Asp
NR_038271.1:n.446+8612T>G (TTN-AS1)
NR_038272.1:n.220-3484T>G (TTN-AS1)
XM_011511729.1:c.103464A>C (TTN)	XP_011510031.1:p.Glu34488Asp
XM_011511730.1:c.77358A>C (TTN)	XP_011510032.1:p.Glu25786Asp
XM_011511731.1:c.77217A>C (TTN)	XP_011510033.1:p.Glu25739Asp
XM_017004819.1:c.103260A>C (TTN)	XP_016860308.1:p.Glu34420Asp
XM_017004820.1:c.98658A>C (TTN)	XP_016860309.1:p.Glu32886Asp
XM_017004821.1:c.98655A>C (TTN)	XP_016860310.1:p.Glu32885Asp
XM_017004822.1:c.95697A>C (TTN)	XP_016860311.1:p.Glu31899Asp
XM_017004823.1:c.77313A>C (TTN)	XP_016860312.1:p.Glu25771Asp
XM_024453094.1:c.98808A>C (TTN)	XP_024308862.1:p.Glu32936Asp
XM_024453095.1:c.98805A>C (TTN)	XP_024308863.1:p.Glu32935Asp
XM_024453096.1:c.98238A>C (TTN)	XP_024308864.1:p.Glu32746Asp
XM_024453097.1:c.95580A>C (TTN)	XP_024308865.1:p.Glu31860Asp
XM_024453098.1:c.95499A>C (TTN)	XP_024308866.1:p.Glu31833Asp
XM_024453099.1:c.77262A>C (TTN)	XP_024308867.1:p.Glu25754Asp
XM_024453100.1:c.67116A>C (TTN)	XP_024308868.1:p.Glu22372Asp