Canonical Allele Identifier: CA1992271

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178589628T>C , CM000664.2:g.178589628T>C	GRCh38
NC_000002.11:g.179454355T>C , CM000664.1:g.179454355T>C	GRCh37
NC_000002.10:g.179162601T>C	NCBI36
NG_011618.3:g.246175A>G , LRG_391:g.246175A>G
NG_051363.1:g.71802T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.62097A>G (TTN) MANE Select	NP_001254479.2:p.Pro20699=
ENST00000589042.5:c.62097A>G (TTN) MANE Select	ENSP00000467141.1:p.Pro20699=
NM_001256850.1:c.57174A>G (TTN)	NP_001243779.1:p.Pro19058=
NM_003319.4:c.34902A>G (TTN)	NP_003310.4:p.Pro11634=
NM_133378.4:c.54393A>G (TTN)	NP_596869.4:p.Pro18131=
NM_133432.3:c.35277A>G (TTN)	NP_597676.3:p.Pro11759=
NM_133437.4:c.35478A>G (TTN)	NP_597681.4:p.Pro11826=
NR_038271.1:n.597-7968T>C (TTN-AS1)
NR_038272.1:n.3189-1511T>C (TTN-AS1)
ENST00000342175.10:c.35478A>G (TTN)	ENSP00000340554.6:p.Pro11826=
ENST00000342175.11:c.35478A>G (TTN)	ENSP00000340554.6:p.Pro11826=
ENST00000342992.10:c.54393A>G (TTN)	ENSP00000343764.6:p.Pro18131=
ENST00000342992.11:c.54393A>G (TTN)	ENSP00000343764.6:p.Pro18131=
ENST00000359218.10:c.35277A>G (TTN)	ENSP00000352154.5:p.Pro11759=
ENST00000359218.9:c.35277A>G (TTN)	ENSP00000352154.5:p.Pro11759=
ENST00000460472.6:c.34902A>G (TTN)	ENSP00000434586.1:p.Pro11634=
ENST00000591111.5:c.57174A>G (TTN)	ENSP00000465570.1:p.Pro19058=
ENST00000615779.4:c.57174A>G (TTN)	ENSP00000483597.1:p.Pro19058=
XM_011511729.1:c.61194A>G (TTN)	XP_011510031.1:p.Pro20398=
XM_011511730.1:c.35088A>G (TTN)	XP_011510032.1:p.Pro11696=
XM_011511731.1:c.34947A>G (TTN)	XP_011510033.1:p.Pro11649=
XM_017004819.1:c.60990A>G (TTN)	XP_016860308.1:p.Pro20330=
XM_017004820.1:c.56388A>G (TTN)	XP_016860309.1:p.Pro18796=
XM_017004821.1:c.56385A>G (TTN)	XP_016860310.1:p.Pro18795=
XM_017004822.1:c.53427A>G (TTN)	XP_016860311.1:p.Pro17809=
XM_017004823.1:c.35043A>G (TTN)	XP_016860312.1:p.Pro11681=
XM_024453094.1:c.56538A>G (TTN)	XP_024308862.1:p.Pro18846=
XM_024453095.1:c.56535A>G (TTN)	XP_024308863.1:p.Pro18845=
XM_024453096.1:c.55968A>G (TTN)	XP_024308864.1:p.Pro18656=
XM_024453097.1:c.53310A>G (TTN)	XP_024308865.1:p.Pro17770=
XM_024453098.1:c.53229A>G (TTN)	XP_024308866.1:p.Pro17743=
XM_024453099.1:c.34992A>G (TTN)	XP_024308867.1:p.Pro11664=
XM_024453100.1:c.24846A>G (TTN)	XP_024308868.1:p.Pro8282=