Canonical Allele Identifier: CA1310508296

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527612G= , CM000664.2:g.178527612G=	GRCh38
NC_000002.11:g.179392339G= , CM000664.1:g.179392339G=	GRCh37
NC_000002.10:g.179100585G=	NCBI36
NG_011618.3:g.308191C= , LRG_391:g.308191C=
NG_051363.1:g.9786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99810C= (TTN)	ENSP00000343764.6:p.Ser33270=
ENST00000342175.11:c.80895C= (TTN)	ENSP00000340554.6:p.Ser26965=
ENST00000359218.10:c.80694C= (TTN)	ENSP00000352154.5:p.Ser26898=
ENST00000342175.10:c.80895C= (TTN)	ENSP00000340554.6:p.Ser26965=
ENST00000342992.10:c.99810C= (TTN)	ENSP00000343764.6:p.Ser33270=
ENST00000359218.9:c.80694C= (TTN)	ENSP00000352154.5:p.Ser26898=
ENST00000460472.6:c.80319C= (TTN)	ENSP00000434586.1:p.Ser26773=
ENST00000589042.5:c.107514C= (TTN) MANE Select	ENSP00000467141.1:p.Ser35838=
ENST00000591111.5:c.102591C= (TTN)	ENSP00000465570.1:p.Ser34197=
ENST00000615779.4:c.102591C= (TTN)	ENSP00000483597.1:p.Ser34197=
NM_001256850.1:c.102591C= (TTN)	NP_001243779.1:p.Ser34197=
NM_001267550.2:c.107514C= (TTN) MANE Select	NP_001254479.2:p.Ser35838=
NM_003319.4:c.80319C= (TTN)	NP_003310.4:p.Ser26773=
NM_133378.4:c.99810C= (TTN)	NP_596869.4:p.Ser33270=
NM_133432.3:c.80694C= (TTN)	NP_597676.3:p.Ser26898=
NM_133437.4:c.80895C= (TTN)	NP_597681.4:p.Ser26965=
NR_038271.1:n.446+3976G= (TTN-AS1)
NR_038272.1:n.219+3976G= (TTN-AS1)
XM_011511729.1:c.106611C= (TTN)	XP_011510031.1:p.Ser35537=
XM_011511730.1:c.80505C= (TTN)	XP_011510032.1:p.Ser26835=
XM_011511731.1:c.80364C= (TTN)	XP_011510033.1:p.Ser26788=
XM_017004819.1:c.106407C= (TTN)	XP_016860308.1:p.Ser35469=
XM_017004820.1:c.101805C= (TTN)	XP_016860309.1:p.Ser33935=
XM_017004821.1:c.101802C= (TTN)	XP_016860310.1:p.Ser33934=
XM_017004822.1:c.98844C= (TTN)	XP_016860311.1:p.Ser32948=
XM_017004823.1:c.80460C= (TTN)	XP_016860312.1:p.Ser26820=
XM_024453094.1:c.101955C= (TTN)	XP_024308862.1:p.Ser33985=
XM_024453095.1:c.101952C= (TTN)	XP_024308863.1:p.Ser33984=
XM_024453096.1:c.101385C= (TTN)	XP_024308864.1:p.Ser33795=
XM_024453097.1:c.98727C= (TTN)	XP_024308865.1:p.Ser32909=
XM_024453098.1:c.98646C= (TTN)	XP_024308866.1:p.Ser32882=
XM_024453099.1:c.80409C= (TTN)	XP_024308867.1:p.Ser26803=
XM_024453100.1:c.70263C= (TTN)	XP_024308868.1:p.Ser23421=