Canonical Allele Identifier: CA349411638

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396870A>T (hg19) ; chr2:g.178532143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532143A>T , CM000664.2:g.178532143A>T	GRCh38
NC_000002.11:g.179396870A>T , CM000664.1:g.179396870A>T	GRCh37
NC_000002.10:g.179105116A>T	NCBI36
NG_011618.3:g.303660T>A , LRG_391:g.303660T>A
NG_051363.1:g.14317A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96768T>A (TTN)	ENSP00000343764.6:p.His32256Gln
ENST00000342175.11:c.77853T>A (TTN)	ENSP00000340554.6:p.His25951Gln
ENST00000359218.10:c.77652T>A (TTN)	ENSP00000352154.5:p.His25884Gln
ENST00000342175.10:c.77853T>A (TTN)	ENSP00000340554.6:p.His25951Gln
ENST00000342992.10:c.96768T>A (TTN)	ENSP00000343764.6:p.His32256Gln
ENST00000359218.9:c.77652T>A (TTN)	ENSP00000352154.5:p.His25884Gln
ENST00000460472.6:c.77277T>A (TTN)	ENSP00000434586.1:p.His25759Gln
ENST00000589042.5:c.104472T>A (TTN) MANE Select	ENSP00000467141.1:p.His34824Gln
ENST00000591111.5:c.99549T>A (TTN)	ENSP00000465570.1:p.His33183Gln
ENST00000615779.4:c.99549T>A (TTN)	ENSP00000483597.1:p.His33183Gln
NM_001256850.1:c.99549T>A (TTN)	NP_001243779.1:p.His33183Gln
NM_001267550.2:c.104472T>A (TTN) MANE Select	NP_001254479.2:p.His34824Gln
NM_003319.4:c.77277T>A (TTN)	NP_003310.4:p.His25759Gln
NM_133378.4:c.96768T>A (TTN)	NP_596869.4:p.His32256Gln
NM_133432.3:c.77652T>A (TTN)	NP_597676.3:p.His25884Gln
NM_133437.4:c.77853T>A (TTN)	NP_597681.4:p.His25951Gln
NR_038271.1:n.446+8507A>T (TTN-AS1)
NR_038272.1:n.220-3589A>T (TTN-AS1)
XM_011511729.1:c.103569T>A (TTN)	XP_011510031.1:p.His34523Gln
XM_011511730.1:c.77463T>A (TTN)	XP_011510032.1:p.His25821Gln
XM_011511731.1:c.77322T>A (TTN)	XP_011510033.1:p.His25774Gln
XM_017004819.1:c.103365T>A (TTN)	XP_016860308.1:p.His34455Gln
XM_017004820.1:c.98763T>A (TTN)	XP_016860309.1:p.His32921Gln
XM_017004821.1:c.98760T>A (TTN)	XP_016860310.1:p.His32920Gln
XM_017004822.1:c.95802T>A (TTN)	XP_016860311.1:p.His31934Gln
XM_017004823.1:c.77418T>A (TTN)	XP_016860312.1:p.His25806Gln
XM_024453094.1:c.98913T>A (TTN)	XP_024308862.1:p.His32971Gln
XM_024453095.1:c.98910T>A (TTN)	XP_024308863.1:p.His32970Gln
XM_024453096.1:c.98343T>A (TTN)	XP_024308864.1:p.His32781Gln
XM_024453097.1:c.95685T>A (TTN)	XP_024308865.1:p.His31895Gln
XM_024453098.1:c.95604T>A (TTN)	XP_024308866.1:p.His31868Gln
XM_024453099.1:c.77367T>A (TTN)	XP_024308867.1:p.His25789Gln
XM_024453100.1:c.67221T>A (TTN)	XP_024308868.1:p.His22407Gln