Canonical Allele Identifier: CA1310511399

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530061A= , CM000664.2:g.178530061A=	GRCh38
NC_000002.11:g.179394788A= , CM000664.1:g.179394788A=	GRCh37
NC_000002.10:g.179103034A=	NCBI36
NG_011618.3:g.305742T= , LRG_391:g.305742T=
NG_051363.1:g.12235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98726T= (TTN)	ENSP00000343764.6:p.Leu32909=
ENST00000342175.11:c.79811T= (TTN)	ENSP00000340554.6:p.Leu26604=
ENST00000359218.10:c.79610T= (TTN)	ENSP00000352154.5:p.Leu26537=
ENST00000342175.10:c.79811T= (TTN)	ENSP00000340554.6:p.Leu26604=
ENST00000342992.10:c.98726T= (TTN)	ENSP00000343764.6:p.Leu32909=
ENST00000359218.9:c.79610T= (TTN)	ENSP00000352154.5:p.Leu26537=
ENST00000460472.6:c.79235T= (TTN)	ENSP00000434586.1:p.Leu26412=
ENST00000589042.5:c.106430T= (TTN) MANE Select	ENSP00000467141.1:p.Leu35477=
ENST00000591111.5:c.101507T= (TTN)	ENSP00000465570.1:p.Leu33836=
ENST00000615779.4:c.101507T= (TTN)	ENSP00000483597.1:p.Leu33836=
NM_001256850.1:c.101507T= (TTN)	NP_001243779.1:p.Leu33836=
NM_001267550.2:c.106430T= (TTN) MANE Select	NP_001254479.2:p.Leu35477=
NM_003319.4:c.79235T= (TTN)	NP_003310.4:p.Leu26412=
NM_133378.4:c.98726T= (TTN)	NP_596869.4:p.Leu32909=
NM_133432.3:c.79610T= (TTN)	NP_597676.3:p.Leu26537=
NM_133437.4:c.79811T= (TTN)	NP_597681.4:p.Leu26604=
NR_038271.1:n.446+6425A= (TTN-AS1)
NR_038272.1:n.220-5671A= (TTN-AS1)
XM_011511729.1:c.105527T= (TTN)	XP_011510031.1:p.Leu35176=
XM_011511730.1:c.79421T= (TTN)	XP_011510032.1:p.Leu26474=
XM_011511731.1:c.79280T= (TTN)	XP_011510033.1:p.Leu26427=
XM_017004819.1:c.105323T= (TTN)	XP_016860308.1:p.Leu35108=
XM_017004820.1:c.100721T= (TTN)	XP_016860309.1:p.Leu33574=
XM_017004821.1:c.100718T= (TTN)	XP_016860310.1:p.Leu33573=
XM_017004822.1:c.97760T= (TTN)	XP_016860311.1:p.Leu32587=
XM_017004823.1:c.79376T= (TTN)	XP_016860312.1:p.Leu26459=
XM_024453094.1:c.100871T= (TTN)	XP_024308862.1:p.Leu33624=
XM_024453095.1:c.100868T= (TTN)	XP_024308863.1:p.Leu33623=
XM_024453096.1:c.100301T= (TTN)	XP_024308864.1:p.Leu33434=
XM_024453097.1:c.97643T= (TTN)	XP_024308865.1:p.Leu32548=
XM_024453098.1:c.97562T= (TTN)	XP_024308866.1:p.Leu32521=
XM_024453099.1:c.79325T= (TTN)	XP_024308867.1:p.Leu26442=
XM_024453100.1:c.69179T= (TTN)	XP_024308868.1:p.Leu23060=