Canonical Allele Identifier: CA349411906

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396980T>C (hg19) ; chr2:g.178532253T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532253T>C , CM000664.2:g.178532253T>C	GRCh38
NC_000002.11:g.179396980T>C , CM000664.1:g.179396980T>C	GRCh37
NC_000002.10:g.179105226T>C	NCBI36
NG_011618.3:g.303550A>G , LRG_391:g.303550A>G
NG_051363.1:g.14427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96658A>G (TTN)	ENSP00000343764.6:p.Ser32220Gly
ENST00000342175.11:c.77743A>G (TTN)	ENSP00000340554.6:p.Ser25915Gly
ENST00000359218.10:c.77542A>G (TTN)	ENSP00000352154.5:p.Ser25848Gly
ENST00000342175.10:c.77743A>G (TTN)	ENSP00000340554.6:p.Ser25915Gly
ENST00000342992.10:c.96658A>G (TTN)	ENSP00000343764.6:p.Ser32220Gly
ENST00000359218.9:c.77542A>G (TTN)	ENSP00000352154.5:p.Ser25848Gly
ENST00000460472.6:c.77167A>G (TTN)	ENSP00000434586.1:p.Ser25723Gly
ENST00000589042.5:c.104362A>G (TTN) MANE Select	ENSP00000467141.1:p.Ser34788Gly
ENST00000591111.5:c.99439A>G (TTN)	ENSP00000465570.1:p.Ser33147Gly
ENST00000615779.4:c.99439A>G (TTN)	ENSP00000483597.1:p.Ser33147Gly
NM_001256850.1:c.99439A>G (TTN)	NP_001243779.1:p.Ser33147Gly
NM_001267550.2:c.104362A>G (TTN) MANE Select	NP_001254479.2:p.Ser34788Gly
NM_003319.4:c.77167A>G (TTN)	NP_003310.4:p.Ser25723Gly
NM_133378.4:c.96658A>G (TTN)	NP_596869.4:p.Ser32220Gly
NM_133432.3:c.77542A>G (TTN)	NP_597676.3:p.Ser25848Gly
NM_133437.4:c.77743A>G (TTN)	NP_597681.4:p.Ser25915Gly
NR_038271.1:n.446+8617T>C (TTN-AS1)
NR_038272.1:n.220-3479T>C (TTN-AS1)
XM_011511729.1:c.103459A>G (TTN)	XP_011510031.1:p.Ser34487Gly
XM_011511730.1:c.77353A>G (TTN)	XP_011510032.1:p.Ser25785Gly
XM_011511731.1:c.77212A>G (TTN)	XP_011510033.1:p.Ser25738Gly
XM_017004819.1:c.103255A>G (TTN)	XP_016860308.1:p.Ser34419Gly
XM_017004820.1:c.98653A>G (TTN)	XP_016860309.1:p.Ser32885Gly
XM_017004821.1:c.98650A>G (TTN)	XP_016860310.1:p.Ser32884Gly
XM_017004822.1:c.95692A>G (TTN)	XP_016860311.1:p.Ser31898Gly
XM_017004823.1:c.77308A>G (TTN)	XP_016860312.1:p.Ser25770Gly
XM_024453094.1:c.98803A>G (TTN)	XP_024308862.1:p.Ser32935Gly
XM_024453095.1:c.98800A>G (TTN)	XP_024308863.1:p.Ser32934Gly
XM_024453096.1:c.98233A>G (TTN)	XP_024308864.1:p.Ser32745Gly
XM_024453097.1:c.95575A>G (TTN)	XP_024308865.1:p.Ser31859Gly
XM_024453098.1:c.95494A>G (TTN)	XP_024308866.1:p.Ser31832Gly
XM_024453099.1:c.77257A>G (TTN)	XP_024308867.1:p.Ser25753Gly
XM_024453100.1:c.67111A>G (TTN)	XP_024308868.1:p.Ser22371Gly