Canonical Allele Identifier: CA1310598718

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178733481T= , CM000664.2:g.178733481T=	GRCh38
NC_000002.11:g.179598208T= , CM000664.1:g.179598208T=	GRCh37
NC_000002.10:g.179306453T=	NCBI36
NG_011618.3:g.102322A= , LRG_391:g.102322A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.12080A=	ENSP00000343764.6:p.Gln4027=
ENST00000342175.11:c.13858+4601A=	ENSP00000340554.6:n.13858+4601A=
ENST00000359218.10:c.13657+4601A=	ENSP00000352154.5:n.13657+4601A=
ENST00000342175.10:c.13858+4601A=	ENSP00000340554.6:n.13858+4601A=
ENST00000342992.10:c.12080A=	ENSP00000343764.6:p.Gln4027=
ENST00000359218.9:c.13657+4601A=	ENSP00000352154.5:n.13657+4601A=
ENST00000460472.6:c.13282+4601A=	ENSP00000434586.1:n.13282+4601A=
ENST00000589042.5:c.15812A= MANE Select	ENSP00000467141.1:p.Gln5271=
ENST00000591111.5:c.14861A=	ENSP00000465570.1:p.Gln4954=
ENST00000615779.4:c.14861A=	ENSP00000483597.1:p.Gln4954=
NM_001256850.1:c.14861A=	NP_001243779.1:p.Gln4954=
NM_001267550.2:c.15812A= MANE Select	NP_001254479.2:p.Gln5271=
NM_003319.4:c.13282+4601A=	NP_003310.4:n.13282+4601A=
NM_133378.4:c.12080A=	NP_596869.4:p.Gln4027=
NM_133432.3:c.13657+4601A=	NP_597676.3:n.13657+4601A=
NM_133437.4:c.13858+4601A=	NP_597681.4:n.13858+4601A=
XM_011511729.1:c.14909A=	XP_011510031.1:p.Gln4970=
XM_011511730.1:c.13468+4601A=	XP_011510032.1:n.13468+4601A=
XM_011511731.1:c.13327+4601A=	XP_011510033.1:n.13327+4601A=
XM_017004819.1:c.14864A=	XP_016860308.1:p.Gln4955=
XM_017004820.1:c.12083A=	XP_016860309.1:p.Gln4028=
XM_017004821.1:c.12080A=	XP_016860310.1:p.Gln4027=
XM_017004822.1:c.14864A=	XP_016860311.1:p.Gln4955=
XM_017004823.1:c.13423+4601A=	XP_016860312.1:n.13423+4601A=
XM_024453094.1:c.14864A=	XP_024308862.1:p.Gln4955=
XM_024453095.1:c.14864A=	XP_024308863.1:p.Gln4955=
XM_024453096.1:c.14864A=	XP_024308864.1:p.Gln4955=
XM_024453097.1:c.14864A=	XP_024308865.1:p.Gln4955=
XM_024453098.1:c.14864A=	XP_024308866.1:p.Gln4955=
XM_024453099.1:c.13423+4601A=	XP_024308867.1:n.13423+4601A=