Canonical Allele Identifier: CA430256672

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178573502T>C , CM000664.2:g.178573502T>C	GRCh38
NC_000002.11:g.179438229T>C , CM000664.1:g.179438229T>C	GRCh37
NC_000002.10:g.179146475T>C	NCBI36
NG_011618.3:g.262301A>G , LRG_391:g.262301A>G
NG_051363.1:g.55676T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.72630A>G (TTN) MANE Select	NP_001254479.2:p.Glu24210=
ENST00000589042.5:c.72630A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu24210=
NM_001256850.1:c.67707A>G (TTN)	NP_001243779.1:p.Glu22569=
NM_003319.4:c.45435A>G (TTN)	NP_003310.4:p.Glu15145=
NM_133378.4:c.64926A>G (TTN)	NP_596869.4:p.Glu21642=
NM_133432.3:c.45810A>G (TTN)	NP_597676.3:p.Glu15270=
NM_133437.4:c.46011A>G (TTN)	NP_597681.4:p.Glu15337=
NR_038271.1:n.596+2053T>C (TTN-AS1)
NR_038272.1:n.2044-9070T>C (TTN-AS1)
ENST00000342175.10:c.46011A>G (TTN)	ENSP00000340554.6:p.Glu15337=
ENST00000342175.11:c.46011A>G (TTN)	ENSP00000340554.6:p.Glu15337=
ENST00000342992.10:c.64926A>G (TTN)	ENSP00000343764.6:p.Glu21642=
ENST00000342992.11:c.64926A>G (TTN)	ENSP00000343764.6:p.Glu21642=
ENST00000359218.10:c.45810A>G (TTN)	ENSP00000352154.5:p.Glu15270=
ENST00000359218.9:c.45810A>G (TTN)	ENSP00000352154.5:p.Glu15270=
ENST00000460472.6:c.45435A>G (TTN)	ENSP00000434586.1:p.Glu15145=
ENST00000591111.5:c.67707A>G (TTN)	ENSP00000465570.1:p.Glu22569=
ENST00000615779.4:c.67707A>G (TTN)	ENSP00000483597.1:p.Glu22569=
XM_011511729.1:c.71727A>G (TTN)	XP_011510031.1:p.Glu23909=
XM_011511730.1:c.45621A>G (TTN)	XP_011510032.1:p.Glu15207=
XM_011511731.1:c.45480A>G (TTN)	XP_011510033.1:p.Glu15160=
XM_017004819.1:c.71523A>G (TTN)	XP_016860308.1:p.Glu23841=
XM_017004820.1:c.66921A>G (TTN)	XP_016860309.1:p.Glu22307=
XM_017004821.1:c.66918A>G (TTN)	XP_016860310.1:p.Glu22306=
XM_017004822.1:c.63960A>G (TTN)	XP_016860311.1:p.Glu21320=
XM_017004823.1:c.45576A>G (TTN)	XP_016860312.1:p.Glu15192=
XM_024453094.1:c.67071A>G (TTN)	XP_024308862.1:p.Glu22357=
XM_024453095.1:c.67068A>G (TTN)	XP_024308863.1:p.Glu22356=
XM_024453096.1:c.66501A>G (TTN)	XP_024308864.1:p.Glu22167=
XM_024453097.1:c.63843A>G (TTN)	XP_024308865.1:p.Glu21281=
XM_024453098.1:c.63762A>G (TTN)	XP_024308866.1:p.Glu21254=
XM_024453099.1:c.45525A>G (TTN)	XP_024308867.1:p.Glu15175=
XM_024453100.1:c.35379A>G (TTN)	XP_024308868.1:p.Glu11793=