Canonical Allele Identifier: CA1310537078

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584569C= , CM000664.2:g.178584569C=	GRCh38
NC_000002.11:g.179449296C= , CM000664.1:g.179449296C=	GRCh37
NC_000002.10:g.179157542C=	NCBI36
NG_011618.3:g.251234G= , LRG_391:g.251234G=
NG_051363.1:g.66743C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57278G= (TTN)	ENSP00000343764.6:p.Ser19093=
ENST00000342175.11:c.38363G= (TTN)	ENSP00000340554.6:p.Ser12788=
ENST00000359218.10:c.38162G= (TTN)	ENSP00000352154.5:p.Ser12721=
ENST00000342175.10:c.38363G= (TTN)	ENSP00000340554.6:p.Ser12788=
ENST00000342992.10:c.57278G= (TTN)	ENSP00000343764.6:p.Ser19093=
ENST00000359218.9:c.38162G= (TTN)	ENSP00000352154.5:p.Ser12721=
ENST00000460472.6:c.37787G= (TTN)	ENSP00000434586.1:p.Ser12596=
ENST00000589042.5:c.64982G= (TTN) MANE Select	ENSP00000467141.1:p.Ser21661=
ENST00000591111.5:c.60059G= (TTN)	ENSP00000465570.1:p.Ser20020=
ENST00000615779.4:c.60059G= (TTN)	ENSP00000483597.1:p.Ser20020=
NM_001256850.1:c.60059G= (TTN)	NP_001243779.1:p.Ser20020=
NM_001267550.2:c.64982G= (TTN) MANE Select	NP_001254479.2:p.Ser21661=
NM_003319.4:c.37787G= (TTN)	NP_003310.4:p.Ser12596=
NM_133378.4:c.57278G= (TTN)	NP_596869.4:p.Ser19093=
NM_133432.3:c.38162G= (TTN)	NP_597676.3:p.Ser12721=
NM_133437.4:c.38363G= (TTN)	NP_597681.4:p.Ser12788=
NR_038271.1:n.597-13027C= (TTN-AS1)
NR_038272.1:n.2768-4C= (TTN-AS1)
XM_011511729.1:c.64079G= (TTN)	XP_011510031.1:p.Ser21360=
XM_011511730.1:c.37973G= (TTN)	XP_011510032.1:p.Ser12658=
XM_011511731.1:c.37832G= (TTN)	XP_011510033.1:p.Ser12611=
XM_017004819.1:c.63875G= (TTN)	XP_016860308.1:p.Ser21292=
XM_017004820.1:c.59273G= (TTN)	XP_016860309.1:p.Ser19758=
XM_017004821.1:c.59270G= (TTN)	XP_016860310.1:p.Ser19757=
XM_017004822.1:c.56312G= (TTN)	XP_016860311.1:p.Ser18771=
XM_017004823.1:c.37928G= (TTN)	XP_016860312.1:p.Ser12643=
XM_024453094.1:c.59423G= (TTN)	XP_024308862.1:p.Ser19808=
XM_024453095.1:c.59420G= (TTN)	XP_024308863.1:p.Ser19807=
XM_024453096.1:c.58853G= (TTN)	XP_024308864.1:p.Ser19618=
XM_024453097.1:c.56195G= (TTN)	XP_024308865.1:p.Ser18732=
XM_024453098.1:c.56114G= (TTN)	XP_024308866.1:p.Ser18705=
XM_024453099.1:c.37877G= (TTN)	XP_024308867.1:p.Ser12626=
XM_024453100.1:c.27731G= (TTN)	XP_024308868.1:p.Ser9244=