Canonical Allele Identifier: CA60984655

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178560639C>T , CM000664.2:g.178560639C>T	GRCh38
NC_000002.11:g.179425366C>T , CM000664.1:g.179425366C>T	GRCh37
NC_000002.10:g.179133612C>T	NCBI36
NG_011618.3:g.275164G>A , LRG_391:g.275164G>A
NG_051363.1:g.42813C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.85493G>A (TTN) MANE Select	NP_001254479.2:p.Trp28498Ter
ENST00000589042.5:c.85493G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp28498Ter
NM_001256850.1:c.80570G>A (TTN)	NP_001243779.1:p.Trp26857Ter
NM_003319.4:c.58298G>A (TTN)	NP_003310.4:p.Trp19433Ter
NM_133378.4:c.77789G>A (TTN)	NP_596869.4:p.Trp25930Ter
NM_133432.3:c.58673G>A (TTN)	NP_597676.3:p.Trp19558Ter
NM_133437.4:c.58874G>A (TTN)	NP_597681.4:p.Trp19625Ter
NR_038271.1:n.447-10661C>T (TTN-AS1)
NR_038272.1:n.2043+18278C>T (TTN-AS1)
ENST00000342175.10:c.58874G>A (TTN)	ENSP00000340554.6:p.Trp19625Ter
ENST00000342175.11:c.58874G>A (TTN)	ENSP00000340554.6:p.Trp19625Ter
ENST00000342992.10:c.77789G>A (TTN)	ENSP00000343764.6:p.Trp25930Ter
ENST00000342992.11:c.77789G>A (TTN)	ENSP00000343764.6:p.Trp25930Ter
ENST00000359218.10:c.58673G>A (TTN)	ENSP00000352154.5:p.Trp19558Ter
ENST00000359218.9:c.58673G>A (TTN)	ENSP00000352154.5:p.Trp19558Ter
ENST00000460472.6:c.58298G>A (TTN)	ENSP00000434586.1:p.Trp19433Ter
ENST00000591111.5:c.80570G>A (TTN)	ENSP00000465570.1:p.Trp26857Ter
ENST00000615779.4:c.80570G>A (TTN)	ENSP00000483597.1:p.Trp26857Ter
XM_011511729.1:c.84590G>A (TTN)	XP_011510031.1:p.Trp28197Ter
XM_011511730.1:c.58484G>A (TTN)	XP_011510032.1:p.Trp19495Ter
XM_011511731.1:c.58343G>A (TTN)	XP_011510033.1:p.Trp19448Ter
XM_017004819.1:c.84386G>A (TTN)	XP_016860308.1:p.Trp28129Ter
XM_017004820.1:c.79784G>A (TTN)	XP_016860309.1:p.Trp26595Ter
XM_017004821.1:c.79781G>A (TTN)	XP_016860310.1:p.Trp26594Ter
XM_017004822.1:c.76823G>A (TTN)	XP_016860311.1:p.Trp25608Ter
XM_017004823.1:c.58439G>A (TTN)	XP_016860312.1:p.Trp19480Ter
XM_024453094.1:c.79934G>A (TTN)	XP_024308862.1:p.Trp26645Ter
XM_024453095.1:c.79931G>A (TTN)	XP_024308863.1:p.Trp26644Ter
XM_024453096.1:c.79364G>A (TTN)	XP_024308864.1:p.Trp26455Ter
XM_024453097.1:c.76706G>A (TTN)	XP_024308865.1:p.Trp25569Ter
XM_024453098.1:c.76625G>A (TTN)	XP_024308866.1:p.Trp25542Ter
XM_024453099.1:c.58388G>A (TTN)	XP_024308867.1:p.Trp19463Ter
XM_024453100.1:c.48242G>A (TTN)	XP_024308868.1:p.Trp16081Ter