Canonical Allele Identifier: CA1310549122

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178613906A= , CM000664.2:g.178613906A=	GRCh38
NC_000002.11:g.179478633A= , CM000664.1:g.179478633A=	GRCh37
NC_000002.10:g.179186878A=	NCBI36
NG_011618.3:g.221897T= , LRG_391:g.221897T=
NG_051363.1:g.96080A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41673T= (TTN)	ENSP00000343764.6:p.Pro13891=
ENST00000342175.11:c.22758T= (TTN)	ENSP00000340554.6:p.Pro7586=
ENST00000359218.10:c.22557T= (TTN)	ENSP00000352154.5:p.Pro7519=
ENST00000342175.10:c.22758T= (TTN)	ENSP00000340554.6:p.Pro7586=
ENST00000342992.10:c.41673T= (TTN)	ENSP00000343764.6:p.Pro13891=
ENST00000359218.9:c.22557T= (TTN)	ENSP00000352154.5:p.Pro7519=
ENST00000460472.6:c.22182T= (TTN)	ENSP00000434586.1:p.Pro7394=
ENST00000589042.5:c.49377T= (TTN) MANE Select	ENSP00000467141.1:p.Pro16459=
ENST00000591111.5:c.44454T= (TTN)	ENSP00000465570.1:p.Pro14818=
ENST00000615779.4:c.44454T= (TTN)	ENSP00000483597.1:p.Pro14818=
NM_001256850.1:c.44454T= (TTN)	NP_001243779.1:p.Pro14818=
NM_001267550.2:c.49377T= (TTN) MANE Select	NP_001254479.2:p.Pro16459=
NM_003319.4:c.22182T= (TTN)	NP_003310.4:p.Pro7394=
NM_133378.4:c.41673T= (TTN)	NP_596869.4:p.Pro13891=
NM_133432.3:c.22557T= (TTN)	NP_597676.3:p.Pro7519=
NM_133437.4:c.22758T= (TTN)	NP_597681.4:p.Pro7586=
NR_038271.1:n.783-129A= (TTN-AS1)
XM_011511729.1:c.48474T= (TTN)	XP_011510031.1:p.Pro16158=
XM_011511730.1:c.22368T= (TTN)	XP_011510032.1:p.Pro7456=
XM_011511731.1:c.22227T= (TTN)	XP_011510033.1:p.Pro7409=
XM_017004819.1:c.48270T= (TTN)	XP_016860308.1:p.Pro16090=
XM_017004820.1:c.43668T= (TTN)	XP_016860309.1:p.Pro14556=
XM_017004821.1:c.43665T= (TTN)	XP_016860310.1:p.Pro14555=
XM_017004822.1:c.40707T= (TTN)	XP_016860311.1:p.Pro13569=
XM_017004823.1:c.22323T= (TTN)	XP_016860312.1:p.Pro7441=
XM_024453094.1:c.43818T= (TTN)	XP_024308862.1:p.Pro14606=
XM_024453095.1:c.43815T= (TTN)	XP_024308863.1:p.Pro14605=
XM_024453096.1:c.43248T= (TTN)	XP_024308864.1:p.Pro14416=
XM_024453097.1:c.40590T= (TTN)	XP_024308865.1:p.Pro13530=
XM_024453098.1:c.40509T= (TTN)	XP_024308866.1:p.Pro13503=
XM_024453099.1:c.22272T= (TTN)	XP_024308867.1:p.Pro7424=
XM_024453100.1:c.12126T= (TTN)	XP_024308868.1:p.Pro4042=