Canonical Allele Identifier: CA430235973

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532287T>G , CM000664.2:g.178532287T>G	GRCh38
NC_000002.11:g.179397014T>G , CM000664.1:g.179397014T>G	GRCh37
NC_000002.10:g.179105260T>G	NCBI36
NG_011618.3:g.303516A>C , LRG_391:g.303516A>C
NG_051363.1:g.14461T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.104328A>C (TTN) MANE Select	NP_001254479.2:p.Pro34776=
ENST00000589042.5:c.104328A>C (TTN) MANE Select	ENSP00000467141.1:p.Pro34776=
NM_001256850.1:c.99405A>C (TTN)	NP_001243779.1:p.Pro33135=
NM_003319.4:c.77133A>C (TTN)	NP_003310.4:p.Pro25711=
NM_133378.4:c.96624A>C (TTN)	NP_596869.4:p.Pro32208=
NM_133432.3:c.77508A>C (TTN)	NP_597676.3:p.Pro25836=
NM_133437.4:c.77709A>C (TTN)	NP_597681.4:p.Pro25903=
NR_038271.1:n.446+8651T>G (TTN-AS1)
NR_038272.1:n.220-3445T>G (TTN-AS1)
ENST00000342175.10:c.77709A>C (TTN)	ENSP00000340554.6:p.Pro25903=
ENST00000342175.11:c.77709A>C (TTN)	ENSP00000340554.6:p.Pro25903=
ENST00000342992.10:c.96624A>C (TTN)	ENSP00000343764.6:p.Pro32208=
ENST00000342992.11:c.96624A>C (TTN)	ENSP00000343764.6:p.Pro32208=
ENST00000359218.10:c.77508A>C (TTN)	ENSP00000352154.5:p.Pro25836=
ENST00000359218.9:c.77508A>C (TTN)	ENSP00000352154.5:p.Pro25836=
ENST00000460472.6:c.77133A>C (TTN)	ENSP00000434586.1:p.Pro25711=
ENST00000591111.5:c.99405A>C (TTN)	ENSP00000465570.1:p.Pro33135=
ENST00000615779.4:c.99405A>C (TTN)	ENSP00000483597.1:p.Pro33135=
XM_011511729.1:c.103425A>C (TTN)	XP_011510031.1:p.Pro34475=
XM_011511730.1:c.77319A>C (TTN)	XP_011510032.1:p.Pro25773=
XM_011511731.1:c.77178A>C (TTN)	XP_011510033.1:p.Pro25726=
XM_017004819.1:c.103221A>C (TTN)	XP_016860308.1:p.Pro34407=
XM_017004820.1:c.98619A>C (TTN)	XP_016860309.1:p.Pro32873=
XM_017004821.1:c.98616A>C (TTN)	XP_016860310.1:p.Pro32872=
XM_017004822.1:c.95658A>C (TTN)	XP_016860311.1:p.Pro31886=
XM_017004823.1:c.77274A>C (TTN)	XP_016860312.1:p.Pro25758=
XM_024453094.1:c.98769A>C (TTN)	XP_024308862.1:p.Pro32923=
XM_024453095.1:c.98766A>C (TTN)	XP_024308863.1:p.Pro32922=
XM_024453096.1:c.98199A>C (TTN)	XP_024308864.1:p.Pro32733=
XM_024453097.1:c.95541A>C (TTN)	XP_024308865.1:p.Pro31847=
XM_024453098.1:c.95460A>C (TTN)	XP_024308866.1:p.Pro31820=
XM_024453099.1:c.77223A>C (TTN)	XP_024308867.1:p.Pro25741=
XM_024453100.1:c.67077A>C (TTN)	XP_024308868.1:p.Pro22359=