Canonical Allele Identifier: CA1310552297

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621649C= , CM000664.2:g.178621649C=	GRCh38
NC_000002.11:g.179486376C= , CM000664.1:g.179486376C=	GRCh37
NC_000002.10:g.179194621C=	NCBI36
NG_011618.3:g.214154G= , LRG_391:g.214154G=
NG_051363.1:g.103823C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.37471G=	ENSP00000343764.6:p.Ala12491=
ENST00000342175.11:c.18556G=	ENSP00000340554.6:p.Ala6186=
ENST00000359218.10:c.18355G=	ENSP00000352154.5:p.Ala6119=
ENST00000342175.10:c.18556G=	ENSP00000340554.6:p.Ala6186=
ENST00000342992.10:c.37471G=	ENSP00000343764.6:p.Ala12491=
ENST00000359218.9:c.18355G=	ENSP00000352154.5:p.Ala6119=
ENST00000460472.6:c.17980G=	ENSP00000434586.1:p.Ala5994=
ENST00000589042.5:c.45175G= MANE Select	ENSP00000467141.1:p.Ala15059=
ENST00000591111.5:c.40252G=	ENSP00000465570.1:p.Ala13418=
ENST00000615779.4:c.40252G=	ENSP00000483597.1:p.Ala13418=
NM_001256850.1:c.40252G=	NP_001243779.1:p.Ala13418=
NM_001267550.2:c.45175G= MANE Select	NP_001254479.2:p.Ala15059=
NM_003319.4:c.17980G=	NP_003310.4:p.Ala5994=
NM_133378.4:c.37471G=	NP_596869.4:p.Ala12491=
NM_133432.3:c.18355G=	NP_597676.3:p.Ala6119=
NM_133437.4:c.18556G=	NP_597681.4:p.Ala6186=
XM_011511729.1:c.44272G=	XP_011510031.1:p.Ala14758=
XM_011511730.1:c.18166G=	XP_011510032.1:p.Ala6056=
XM_011511731.1:c.18025G=	XP_011510033.1:p.Ala6009=
XM_017004819.1:c.44068G=	XP_016860308.1:p.Ala14690=
XM_017004820.1:c.39466G=	XP_016860309.1:p.Ala13156=
XM_017004821.1:c.39463G=	XP_016860310.1:p.Ala13155=
XM_017004822.1:c.36505G=	XP_016860311.1:p.Ala12169=
XM_017004823.1:c.18121G=	XP_016860312.1:p.Ala6041=
XM_024453094.1:c.39616G=	XP_024308862.1:p.Ala13206=
XM_024453095.1:c.39613G=	XP_024308863.1:p.Ala13205=
XM_024453096.1:c.39046G=	XP_024308864.1:p.Ala13016=
XM_024453097.1:c.36388G=	XP_024308865.1:p.Ala12130=
XM_024453098.1:c.36307G=	XP_024308866.1:p.Ala12103=
XM_024453099.1:c.18070G=	XP_024308867.1:p.Ala6024=
XM_024453100.1:c.7924G=	XP_024308868.1:p.Ala2642=