Canonical Allele Identifier: CA349544197

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178602118G>A , CM000664.2:g.178602118G>A	GRCh38
NC_000002.11:g.179466845G>A , CM000664.1:g.179466845G>A	GRCh37
NC_000002.10:g.179175090G>A	NCBI36
NG_011618.3:g.233685C>T , LRG_391:g.233685C>T
NG_051363.1:g.84292G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.55153C>T (TTN) MANE Select	NP_001254479.2:p.Gln18385Ter
ENST00000589042.5:c.55153C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln18385Ter
NM_001256850.1:c.50230C>T (TTN)	NP_001243779.1:p.Gln16744Ter
NM_003319.4:c.27958C>T (TTN)	NP_003310.4:p.Gln9320Ter
NM_133378.4:c.47449C>T (TTN)	NP_596869.4:p.Gln15817Ter
NM_133432.3:c.28333C>T (TTN)	NP_597676.3:p.Gln9445Ter
NM_133437.4:c.28534C>T (TTN)	NP_597681.4:p.Gln9512Ter
NR_038271.1:n.682+4437G>A (TTN-AS1)
NR_038272.1:n.3917+1451G>A (TTN-AS1)
ENST00000342175.10:c.28534C>T (TTN)	ENSP00000340554.6:p.Gln9512Ter
ENST00000342175.11:c.28534C>T (TTN)	ENSP00000340554.6:p.Gln9512Ter
ENST00000342992.10:c.47449C>T (TTN)	ENSP00000343764.6:p.Gln15817Ter
ENST00000342992.11:c.47449C>T (TTN)	ENSP00000343764.6:p.Gln15817Ter
ENST00000359218.10:c.28333C>T (TTN)	ENSP00000352154.5:p.Gln9445Ter
ENST00000359218.9:c.28333C>T (TTN)	ENSP00000352154.5:p.Gln9445Ter
ENST00000460472.6:c.27958C>T (TTN)	ENSP00000434586.1:p.Gln9320Ter
ENST00000591111.5:c.50230C>T (TTN)	ENSP00000465570.1:p.Gln16744Ter
ENST00000615779.4:c.50230C>T (TTN)	ENSP00000483597.1:p.Gln16744Ter
XM_011511729.1:c.54250C>T (TTN)	XP_011510031.1:p.Gln18084Ter
XM_011511730.1:c.28144C>T (TTN)	XP_011510032.1:p.Gln9382Ter
XM_011511731.1:c.28003C>T (TTN)	XP_011510033.1:p.Gln9335Ter
XM_017004819.1:c.54046C>T (TTN)	XP_016860308.1:p.Gln18016Ter
XM_017004820.1:c.49444C>T (TTN)	XP_016860309.1:p.Gln16482Ter
XM_017004821.1:c.49441C>T (TTN)	XP_016860310.1:p.Gln16481Ter
XM_017004822.1:c.46483C>T (TTN)	XP_016860311.1:p.Gln15495Ter
XM_017004823.1:c.28099C>T (TTN)	XP_016860312.1:p.Gln9367Ter
XM_024453094.1:c.49594C>T (TTN)	XP_024308862.1:p.Gln16532Ter
XM_024453095.1:c.49591C>T (TTN)	XP_024308863.1:p.Gln16531Ter
XM_024453096.1:c.49024C>T (TTN)	XP_024308864.1:p.Gln16342Ter
XM_024453097.1:c.46366C>T (TTN)	XP_024308865.1:p.Gln15456Ter
XM_024453098.1:c.46285C>T (TTN)	XP_024308866.1:p.Gln15429Ter
XM_024453099.1:c.28048C>T (TTN)	XP_024308867.1:p.Gln9350Ter
XM_024453100.1:c.17902C>T (TTN)	XP_024308868.1:p.Gln5968Ter