Canonical Allele Identifier: CA349401413

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178528367G>A , CM000664.2:g.178528367G>A	GRCh38
NC_000002.11:g.179393094G>A , CM000664.1:g.179393094G>A	GRCh37
NC_000002.10:g.179101340G>A	NCBI36
NG_011618.3:g.307436C>T , LRG_391:g.307436C>T
NG_051363.1:g.10541G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107284C>T (TTN) MANE Select	NP_001254479.2:p.Arg35762Ter
ENST00000589042.5:c.107284C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg35762Ter
NM_001256850.1:c.102361C>T (TTN)	NP_001243779.1:p.Arg34121Ter
NM_003319.4:c.80089C>T (TTN)	NP_003310.4:p.Arg26697Ter
NM_133378.4:c.99580C>T (TTN)	NP_596869.4:p.Arg33194Ter
NM_133432.3:c.80464C>T (TTN)	NP_597676.3:p.Arg26822Ter
NM_133437.4:c.80665C>T (TTN)	NP_597681.4:p.Arg26889Ter
NR_038271.1:n.446+4731G>A (TTN-AS1)
NR_038272.1:n.219+4731G>A (TTN-AS1)
ENST00000342175.10:c.80665C>T (TTN)	ENSP00000340554.6:p.Arg26889Ter
ENST00000342175.11:c.80665C>T (TTN)	ENSP00000340554.6:p.Arg26889Ter
ENST00000342992.10:c.99580C>T (TTN)	ENSP00000343764.6:p.Arg33194Ter
ENST00000342992.11:c.99580C>T (TTN)	ENSP00000343764.6:p.Arg33194Ter
ENST00000359218.10:c.80464C>T (TTN)	ENSP00000352154.5:p.Arg26822Ter
ENST00000359218.9:c.80464C>T (TTN)	ENSP00000352154.5:p.Arg26822Ter
ENST00000460472.6:c.80089C>T (TTN)	ENSP00000434586.1:p.Arg26697Ter
ENST00000591111.5:c.102361C>T (TTN)	ENSP00000465570.1:p.Arg34121Ter
ENST00000615779.4:c.102361C>T (TTN)	ENSP00000483597.1:p.Arg34121Ter
XM_011511729.1:c.106381C>T (TTN)	XP_011510031.1:p.Arg35461Ter
XM_011511730.1:c.80275C>T (TTN)	XP_011510032.1:p.Arg26759Ter
XM_011511731.1:c.80134C>T (TTN)	XP_011510033.1:p.Arg26712Ter
XM_017004819.1:c.106177C>T (TTN)	XP_016860308.1:p.Arg35393Ter
XM_017004820.1:c.101575C>T (TTN)	XP_016860309.1:p.Arg33859Ter
XM_017004821.1:c.101572C>T (TTN)	XP_016860310.1:p.Arg33858Ter
XM_017004822.1:c.98614C>T (TTN)	XP_016860311.1:p.Arg32872Ter
XM_017004823.1:c.80230C>T (TTN)	XP_016860312.1:p.Arg26744Ter
XM_024453094.1:c.101725C>T (TTN)	XP_024308862.1:p.Arg33909Ter
XM_024453095.1:c.101722C>T (TTN)	XP_024308863.1:p.Arg33908Ter
XM_024453096.1:c.101155C>T (TTN)	XP_024308864.1:p.Arg33719Ter
XM_024453097.1:c.98497C>T (TTN)	XP_024308865.1:p.Arg32833Ter
XM_024453098.1:c.98416C>T (TTN)	XP_024308866.1:p.Arg32806Ter
XM_024453099.1:c.80179C>T (TTN)	XP_024308867.1:p.Arg26727Ter
XM_024453100.1:c.70033C>T (TTN)	XP_024308868.1:p.Arg23345Ter