Canonical Allele Identifier: CA349502732

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179416387T>C (hg19) ; chr2:g.178551660T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551660T>C , CM000664.2:g.178551660T>C	GRCh38
NC_000002.11:g.179416387T>C , CM000664.1:g.179416387T>C	GRCh37
NC_000002.10:g.179124633T>C	NCBI36
NG_011618.3:g.284143A>G , LRG_391:g.284143A>G
NG_051363.1:g.33834T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.83536A>G (TTN)	ENSP00000343764.6:p.Ser27846Gly
ENST00000342175.11:c.64621A>G (TTN)	ENSP00000340554.6:p.Ser21541Gly
ENST00000359218.10:c.64420A>G (TTN)	ENSP00000352154.5:p.Ser21474Gly
ENST00000342175.10:c.64621A>G (TTN)	ENSP00000340554.6:p.Ser21541Gly
ENST00000342992.10:c.83536A>G (TTN)	ENSP00000343764.6:p.Ser27846Gly
ENST00000359218.9:c.64420A>G (TTN)	ENSP00000352154.5:p.Ser21474Gly
ENST00000460472.6:c.64045A>G (TTN)	ENSP00000434586.1:p.Ser21349Gly
ENST00000589042.5:c.91240A>G (TTN) MANE Select	ENSP00000467141.1:p.Ser30414Gly
ENST00000591111.5:c.86317A>G (TTN)	ENSP00000465570.1:p.Ser28773Gly
ENST00000615779.4:c.86317A>G (TTN)	ENSP00000483597.1:p.Ser28773Gly
NM_001256850.1:c.86317A>G (TTN)	NP_001243779.1:p.Ser28773Gly
NM_001267550.2:c.91240A>G (TTN) MANE Select	NP_001254479.2:p.Ser30414Gly
NM_003319.4:c.64045A>G (TTN)	NP_003310.4:p.Ser21349Gly
NM_133378.4:c.83536A>G (TTN)	NP_596869.4:p.Ser27846Gly
NM_133432.3:c.64420A>G (TTN)	NP_597676.3:p.Ser21474Gly
NM_133437.4:c.64621A>G (TTN)	NP_597681.4:p.Ser21541Gly
NR_038271.1:n.447-19640T>C (TTN-AS1)
NR_038272.1:n.2043+9299T>C (TTN-AS1)
XM_011511729.1:c.90337A>G (TTN)	XP_011510031.1:p.Ser30113Gly
XM_011511730.1:c.64231A>G (TTN)	XP_011510032.1:p.Ser21411Gly
XM_011511731.1:c.64090A>G (TTN)	XP_011510033.1:p.Ser21364Gly
XM_017004819.1:c.90133A>G (TTN)	XP_016860308.1:p.Ser30045Gly
XM_017004820.1:c.85531A>G (TTN)	XP_016860309.1:p.Ser28511Gly
XM_017004821.1:c.85528A>G (TTN)	XP_016860310.1:p.Ser28510Gly
XM_017004822.1:c.82570A>G (TTN)	XP_016860311.1:p.Ser27524Gly
XM_017004823.1:c.64186A>G (TTN)	XP_016860312.1:p.Ser21396Gly
XM_024453094.1:c.85681A>G (TTN)	XP_024308862.1:p.Ser28561Gly
XM_024453095.1:c.85678A>G (TTN)	XP_024308863.1:p.Ser28560Gly
XM_024453096.1:c.85111A>G (TTN)	XP_024308864.1:p.Ser28371Gly
XM_024453097.1:c.82453A>G (TTN)	XP_024308865.1:p.Ser27485Gly
XM_024453098.1:c.82372A>G (TTN)	XP_024308866.1:p.Ser27458Gly
XM_024453099.1:c.64135A>G (TTN)	XP_024308867.1:p.Ser21379Gly
XM_024453100.1:c.53989A>G (TTN)	XP_024308868.1:p.Ser17997Gly