Canonical Allele Identifier: CA430264797

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178587957T>C , CM000664.2:g.178587957T>C	GRCh38
NC_000002.11:g.179452684T>C , CM000664.1:g.179452684T>C	GRCh37
NC_000002.10:g.179160930T>C	NCBI36
NG_011618.3:g.247846A>G , LRG_391:g.247846A>G
NG_051363.1:g.70131T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.63450A>G (TTN) MANE Select	NP_001254479.2:p.Gln21150=
ENST00000589042.5:c.63450A>G (TTN) MANE Select	ENSP00000467141.1:p.Gln21150=
NM_001256850.1:c.58527A>G (TTN)	NP_001243779.1:p.Gln19509=
NM_003319.4:c.36255A>G (TTN)	NP_003310.4:p.Gln12085=
NM_133378.4:c.55746A>G (TTN)	NP_596869.4:p.Gln18582=
NM_133432.3:c.36630A>G (TTN)	NP_597676.3:p.Gln12210=
NM_133437.4:c.36831A>G (TTN)	NP_597681.4:p.Gln12277=
NR_038271.1:n.597-9639T>C (TTN-AS1)
NR_038272.1:n.3188+2964T>C (TTN-AS1)
ENST00000342175.10:c.36831A>G (TTN)	ENSP00000340554.6:p.Gln12277=
ENST00000342175.11:c.36831A>G (TTN)	ENSP00000340554.6:p.Gln12277=
ENST00000342992.10:c.55746A>G (TTN)	ENSP00000343764.6:p.Gln18582=
ENST00000342992.11:c.55746A>G (TTN)	ENSP00000343764.6:p.Gln18582=
ENST00000359218.10:c.36630A>G (TTN)	ENSP00000352154.5:p.Gln12210=
ENST00000359218.9:c.36630A>G (TTN)	ENSP00000352154.5:p.Gln12210=
ENST00000460472.6:c.36255A>G (TTN)	ENSP00000434586.1:p.Gln12085=
ENST00000591111.5:c.58527A>G (TTN)	ENSP00000465570.1:p.Gln19509=
ENST00000615779.4:c.58527A>G (TTN)	ENSP00000483597.1:p.Gln19509=
XM_011511729.1:c.62547A>G (TTN)	XP_011510031.1:p.Gln20849=
XM_011511730.1:c.36441A>G (TTN)	XP_011510032.1:p.Gln12147=
XM_011511731.1:c.36300A>G (TTN)	XP_011510033.1:p.Gln12100=
XM_017004819.1:c.62343A>G (TTN)	XP_016860308.1:p.Gln20781=
XM_017004820.1:c.57741A>G (TTN)	XP_016860309.1:p.Gln19247=
XM_017004821.1:c.57738A>G (TTN)	XP_016860310.1:p.Gln19246=
XM_017004822.1:c.54780A>G (TTN)	XP_016860311.1:p.Gln18260=
XM_017004823.1:c.36396A>G (TTN)	XP_016860312.1:p.Gln12132=
XM_024453094.1:c.57891A>G (TTN)	XP_024308862.1:p.Gln19297=
XM_024453095.1:c.57888A>G (TTN)	XP_024308863.1:p.Gln19296=
XM_024453096.1:c.57321A>G (TTN)	XP_024308864.1:p.Gln19107=
XM_024453097.1:c.54663A>G (TTN)	XP_024308865.1:p.Gln18221=
XM_024453098.1:c.54582A>G (TTN)	XP_024308866.1:p.Gln18194=
XM_024453099.1:c.36345A>G (TTN)	XP_024308867.1:p.Gln12115=
XM_024453100.1:c.26199A>G (TTN)	XP_024308868.1:p.Gln8733=