Canonical Allele Identifier: CA1310518140

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532238T= , CM000664.2:g.178532238T=	GRCh38
NC_000002.11:g.179396965T= , CM000664.1:g.179396965T=	GRCh37
NC_000002.10:g.179105211T=	NCBI36
NG_011618.3:g.303565A= , LRG_391:g.303565A=
NG_051363.1:g.14412T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96673A= (TTN)	ENSP00000343764.6:p.Met32225=
ENST00000342175.11:c.77758A= (TTN)	ENSP00000340554.6:p.Met25920=
ENST00000359218.10:c.77557A= (TTN)	ENSP00000352154.5:p.Met25853=
ENST00000342175.10:c.77758A= (TTN)	ENSP00000340554.6:p.Met25920=
ENST00000342992.10:c.96673A= (TTN)	ENSP00000343764.6:p.Met32225=
ENST00000359218.9:c.77557A= (TTN)	ENSP00000352154.5:p.Met25853=
ENST00000460472.6:c.77182A= (TTN)	ENSP00000434586.1:p.Met25728=
ENST00000589042.5:c.104377A= (TTN) MANE Select	ENSP00000467141.1:p.Met34793=
ENST00000591111.5:c.99454A= (TTN)	ENSP00000465570.1:p.Met33152=
ENST00000615779.4:c.99454A= (TTN)	ENSP00000483597.1:p.Met33152=
NM_001256850.1:c.99454A= (TTN)	NP_001243779.1:p.Met33152=
NM_001267550.2:c.104377A= (TTN) MANE Select	NP_001254479.2:p.Met34793=
NM_003319.4:c.77182A= (TTN)	NP_003310.4:p.Met25728=
NM_133378.4:c.96673A= (TTN)	NP_596869.4:p.Met32225=
NM_133432.3:c.77557A= (TTN)	NP_597676.3:p.Met25853=
NM_133437.4:c.77758A= (TTN)	NP_597681.4:p.Met25920=
NR_038271.1:n.446+8602T= (TTN-AS1)
NR_038272.1:n.220-3494T= (TTN-AS1)
XM_011511729.1:c.103474A= (TTN)	XP_011510031.1:p.Met34492=
XM_011511730.1:c.77368A= (TTN)	XP_011510032.1:p.Met25790=
XM_011511731.1:c.77227A= (TTN)	XP_011510033.1:p.Met25743=
XM_017004819.1:c.103270A= (TTN)	XP_016860308.1:p.Met34424=
XM_017004820.1:c.98668A= (TTN)	XP_016860309.1:p.Met32890=
XM_017004821.1:c.98665A= (TTN)	XP_016860310.1:p.Met32889=
XM_017004822.1:c.95707A= (TTN)	XP_016860311.1:p.Met31903=
XM_017004823.1:c.77323A= (TTN)	XP_016860312.1:p.Met25775=
XM_024453094.1:c.98818A= (TTN)	XP_024308862.1:p.Met32940=
XM_024453095.1:c.98815A= (TTN)	XP_024308863.1:p.Met32939=
XM_024453096.1:c.98248A= (TTN)	XP_024308864.1:p.Met32750=
XM_024453097.1:c.95590A= (TTN)	XP_024308865.1:p.Met31864=
XM_024453098.1:c.95509A= (TTN)	XP_024308866.1:p.Met31837=
XM_024453099.1:c.77272A= (TTN)	XP_024308867.1:p.Met25758=
XM_024453100.1:c.67126A= (TTN)	XP_024308868.1:p.Met22376=