Canonical Allele Identifier: CA349599777

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178612509C>T , CM000664.2:g.178612509C>T	GRCh38
NC_000002.11:g.179477236C>T , CM000664.1:g.179477236C>T	GRCh37
NC_000002.10:g.179185481C>T	NCBI36
NG_011618.3:g.223294G>A , LRG_391:g.223294G>A
NG_051363.1:g.94683C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.50016G>A (TTN) MANE Select	NP_001254479.2:p.Trp16672Ter
ENST00000589042.5:c.50016G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp16672Ter
NM_001256850.1:c.45093G>A (TTN)	NP_001243779.1:p.Trp15031Ter
NM_003319.4:c.22821G>A (TTN)	NP_003310.4:p.Trp7607Ter
NM_133378.4:c.42312G>A (TTN)	NP_596869.4:p.Trp14104Ter
NM_133432.3:c.23196G>A (TTN)	NP_597676.3:p.Trp7732Ter
NM_133437.4:c.23397G>A (TTN)	NP_597681.4:p.Trp7799Ter
NR_038271.1:n.783-1526C>T (TTN-AS1)
ENST00000342175.10:c.23397G>A (TTN)	ENSP00000340554.6:p.Trp7799Ter
ENST00000342175.11:c.23397G>A (TTN)	ENSP00000340554.6:p.Trp7799Ter
ENST00000342992.10:c.42312G>A (TTN)	ENSP00000343764.6:p.Trp14104Ter
ENST00000342992.11:c.42312G>A (TTN)	ENSP00000343764.6:p.Trp14104Ter
ENST00000359218.10:c.23196G>A (TTN)	ENSP00000352154.5:p.Trp7732Ter
ENST00000359218.9:c.23196G>A (TTN)	ENSP00000352154.5:p.Trp7732Ter
ENST00000460472.6:c.22821G>A (TTN)	ENSP00000434586.1:p.Trp7607Ter
ENST00000591111.5:c.45093G>A (TTN)	ENSP00000465570.1:p.Trp15031Ter
ENST00000615779.4:c.45093G>A (TTN)	ENSP00000483597.1:p.Trp15031Ter
XM_011511729.1:c.49113G>A (TTN)	XP_011510031.1:p.Trp16371Ter
XM_011511730.1:c.23007G>A (TTN)	XP_011510032.1:p.Trp7669Ter
XM_011511731.1:c.22866G>A (TTN)	XP_011510033.1:p.Trp7622Ter
XM_017004819.1:c.48909G>A (TTN)	XP_016860308.1:p.Trp16303Ter
XM_017004820.1:c.44307G>A (TTN)	XP_016860309.1:p.Trp14769Ter
XM_017004821.1:c.44304G>A (TTN)	XP_016860310.1:p.Trp14768Ter
XM_017004822.1:c.41346G>A (TTN)	XP_016860311.1:p.Trp13782Ter
XM_017004823.1:c.22962G>A (TTN)	XP_016860312.1:p.Trp7654Ter
XM_024453094.1:c.44457G>A (TTN)	XP_024308862.1:p.Trp14819Ter
XM_024453095.1:c.44454G>A (TTN)	XP_024308863.1:p.Trp14818Ter
XM_024453096.1:c.43887G>A (TTN)	XP_024308864.1:p.Trp14629Ter
XM_024453097.1:c.41229G>A (TTN)	XP_024308865.1:p.Trp13743Ter
XM_024453098.1:c.41148G>A (TTN)	XP_024308866.1:p.Trp13716Ter
XM_024453099.1:c.22911G>A (TTN)	XP_024308867.1:p.Trp7637Ter
XM_024453100.1:c.12765G>A (TTN)	XP_024308868.1:p.Trp4255Ter