Canonical Allele Identifier: CA349411909

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396981T>G (hg19) ; chr2:g.178532254T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532254T>G , CM000664.2:g.178532254T>G	GRCh38
NC_000002.11:g.179396981T>G , CM000664.1:g.179396981T>G	GRCh37
NC_000002.10:g.179105227T>G	NCBI36
NG_011618.3:g.303549A>C , LRG_391:g.303549A>C
NG_051363.1:g.14428T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96657A>C (TTN)	ENSP00000343764.6:p.Lys32219Asn
ENST00000342175.11:c.77742A>C (TTN)	ENSP00000340554.6:p.Lys25914Asn
ENST00000359218.10:c.77541A>C (TTN)	ENSP00000352154.5:p.Lys25847Asn
ENST00000342175.10:c.77742A>C (TTN)	ENSP00000340554.6:p.Lys25914Asn
ENST00000342992.10:c.96657A>C (TTN)	ENSP00000343764.6:p.Lys32219Asn
ENST00000359218.9:c.77541A>C (TTN)	ENSP00000352154.5:p.Lys25847Asn
ENST00000460472.6:c.77166A>C (TTN)	ENSP00000434586.1:p.Lys25722Asn
ENST00000589042.5:c.104361A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys34787Asn
ENST00000591111.5:c.99438A>C (TTN)	ENSP00000465570.1:p.Lys33146Asn
ENST00000615779.4:c.99438A>C (TTN)	ENSP00000483597.1:p.Lys33146Asn
NM_001256850.1:c.99438A>C (TTN)	NP_001243779.1:p.Lys33146Asn
NM_001267550.2:c.104361A>C (TTN) MANE Select	NP_001254479.2:p.Lys34787Asn
NM_003319.4:c.77166A>C (TTN)	NP_003310.4:p.Lys25722Asn
NM_133378.4:c.96657A>C (TTN)	NP_596869.4:p.Lys32219Asn
NM_133432.3:c.77541A>C (TTN)	NP_597676.3:p.Lys25847Asn
NM_133437.4:c.77742A>C (TTN)	NP_597681.4:p.Lys25914Asn
NR_038271.1:n.446+8618T>G (TTN-AS1)
NR_038272.1:n.220-3478T>G (TTN-AS1)
XM_011511729.1:c.103458A>C (TTN)	XP_011510031.1:p.Lys34486Asn
XM_011511730.1:c.77352A>C (TTN)	XP_011510032.1:p.Lys25784Asn
XM_011511731.1:c.77211A>C (TTN)	XP_011510033.1:p.Lys25737Asn
XM_017004819.1:c.103254A>C (TTN)	XP_016860308.1:p.Lys34418Asn
XM_017004820.1:c.98652A>C (TTN)	XP_016860309.1:p.Lys32884Asn
XM_017004821.1:c.98649A>C (TTN)	XP_016860310.1:p.Lys32883Asn
XM_017004822.1:c.95691A>C (TTN)	XP_016860311.1:p.Lys31897Asn
XM_017004823.1:c.77307A>C (TTN)	XP_016860312.1:p.Lys25769Asn
XM_024453094.1:c.98802A>C (TTN)	XP_024308862.1:p.Lys32934Asn
XM_024453095.1:c.98799A>C (TTN)	XP_024308863.1:p.Lys32933Asn
XM_024453096.1:c.98232A>C (TTN)	XP_024308864.1:p.Lys32744Asn
XM_024453097.1:c.95574A>C (TTN)	XP_024308865.1:p.Lys31858Asn
XM_024453098.1:c.95493A>C (TTN)	XP_024308866.1:p.Lys31831Asn
XM_024453099.1:c.77256A>C (TTN)	XP_024308867.1:p.Lys25752Asn
XM_024453100.1:c.67110A>C (TTN)	XP_024308868.1:p.Lys22370Asn