Canonical Allele Identifier: CA349601420

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178613021G>T , CM000664.2:g.178613021G>T	GRCh38
NC_000002.11:g.179477748G>T , CM000664.1:g.179477748G>T	GRCh37
NC_000002.10:g.179185993G>T	NCBI36
NG_011618.3:g.222782C>A , LRG_391:g.222782C>A
NG_051363.1:g.95195G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.49700C>A (TTN) MANE Select	NP_001254479.2:p.Ser16567Ter
ENST00000589042.5:c.49700C>A (TTN) MANE Select	ENSP00000467141.1:p.Ser16567Ter
NM_001256850.1:c.44777C>A (TTN)	NP_001243779.1:p.Ser14926Ter
NM_003319.4:c.22505C>A (TTN)	NP_003310.4:p.Ser7502Ter
NM_133378.4:c.41996C>A (TTN)	NP_596869.4:p.Ser13999Ter
NM_133432.3:c.22880C>A (TTN)	NP_597676.3:p.Ser7627Ter
NM_133437.4:c.23081C>A (TTN)	NP_597681.4:p.Ser7694Ter
NR_038271.1:n.783-1014G>T (TTN-AS1)
ENST00000342175.10:c.23081C>A (TTN)	ENSP00000340554.6:p.Ser7694Ter
ENST00000342175.11:c.23081C>A (TTN)	ENSP00000340554.6:p.Ser7694Ter
ENST00000342992.10:c.41996C>A (TTN)	ENSP00000343764.6:p.Ser13999Ter
ENST00000342992.11:c.41996C>A (TTN)	ENSP00000343764.6:p.Ser13999Ter
ENST00000359218.10:c.22880C>A (TTN)	ENSP00000352154.5:p.Ser7627Ter
ENST00000359218.9:c.22880C>A (TTN)	ENSP00000352154.5:p.Ser7627Ter
ENST00000460472.6:c.22505C>A (TTN)	ENSP00000434586.1:p.Ser7502Ter
ENST00000591111.5:c.44777C>A (TTN)	ENSP00000465570.1:p.Ser14926Ter
ENST00000615779.4:c.44777C>A (TTN)	ENSP00000483597.1:p.Ser14926Ter
XM_011511729.1:c.48797C>A (TTN)	XP_011510031.1:p.Ser16266Ter
XM_011511730.1:c.22691C>A (TTN)	XP_011510032.1:p.Ser7564Ter
XM_011511731.1:c.22550C>A (TTN)	XP_011510033.1:p.Ser7517Ter
XM_017004819.1:c.48593C>A (TTN)	XP_016860308.1:p.Ser16198Ter
XM_017004820.1:c.43991C>A (TTN)	XP_016860309.1:p.Ser14664Ter
XM_017004821.1:c.43988C>A (TTN)	XP_016860310.1:p.Ser14663Ter
XM_017004822.1:c.41030C>A (TTN)	XP_016860311.1:p.Ser13677Ter
XM_017004823.1:c.22646C>A (TTN)	XP_016860312.1:p.Ser7549Ter
XM_024453094.1:c.44141C>A (TTN)	XP_024308862.1:p.Ser14714Ter
XM_024453095.1:c.44138C>A (TTN)	XP_024308863.1:p.Ser14713Ter
XM_024453096.1:c.43571C>A (TTN)	XP_024308864.1:p.Ser14524Ter
XM_024453097.1:c.40913C>A (TTN)	XP_024308865.1:p.Ser13638Ter
XM_024453098.1:c.40832C>A (TTN)	XP_024308866.1:p.Ser13611Ter
XM_024453099.1:c.22595C>A (TTN)	XP_024308867.1:p.Ser7532Ter
XM_024453100.1:c.12449C>A (TTN)	XP_024308868.1:p.Ser4150Ter