Canonical Allele Identifier: CA349472630

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178546876-C-A
• MyVariant Identifiers: chr2:g.179411603C>A (hg19) ; chr2:g.178546876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546876C>A , CM000664.2:g.178546876C>A	GRCh38
NC_000002.11:g.179411603C>A , CM000664.1:g.179411603C>A	GRCh37
NC_000002.10:g.179119849C>A	NCBI36
NG_011618.3:g.288927G>T , LRG_391:g.288927G>T
NG_051363.1:g.29050C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86848G>T (TTN)	ENSP00000343764.6:p.Val28950Phe
ENST00000342175.11:c.67933G>T (TTN)	ENSP00000340554.6:p.Val22645Phe
ENST00000359218.10:c.67732G>T (TTN)	ENSP00000352154.5:p.Val22578Phe
ENST00000342175.10:c.67933G>T (TTN)	ENSP00000340554.6:p.Val22645Phe
ENST00000342992.10:c.86848G>T (TTN)	ENSP00000343764.6:p.Val28950Phe
ENST00000359218.9:c.67732G>T (TTN)	ENSP00000352154.5:p.Val22578Phe
ENST00000460472.6:c.67357G>T (TTN)	ENSP00000434586.1:p.Val22453Phe
ENST00000589042.5:c.94552G>T (TTN) MANE Select	ENSP00000467141.1:p.Val31518Phe
ENST00000591111.5:c.89629G>T (TTN)	ENSP00000465570.1:p.Val29877Phe
ENST00000615779.4:c.89629G>T (TTN)	ENSP00000483597.1:p.Val29877Phe
NM_001256850.1:c.89629G>T (TTN)	NP_001243779.1:p.Val29877Phe
NM_001267550.2:c.94552G>T (TTN) MANE Select	NP_001254479.2:p.Val31518Phe
NM_003319.4:c.67357G>T (TTN)	NP_003310.4:p.Val22453Phe
NM_133378.4:c.86848G>T (TTN)	NP_596869.4:p.Val28950Phe
NM_133432.3:c.67732G>T (TTN)	NP_597676.3:p.Val22578Phe
NM_133437.4:c.67933G>T (TTN)	NP_597681.4:p.Val22645Phe
NR_038271.1:n.446+23240C>A (TTN-AS1)
NR_038272.1:n.2043+4515C>A (TTN-AS1)
XM_011511729.1:c.93649G>T (TTN)	XP_011510031.1:p.Val31217Phe
XM_011511730.1:c.67543G>T (TTN)	XP_011510032.1:p.Val22515Phe
XM_011511731.1:c.67402G>T (TTN)	XP_011510033.1:p.Val22468Phe
XM_017004819.1:c.93445G>T (TTN)	XP_016860308.1:p.Val31149Phe
XM_017004820.1:c.88843G>T (TTN)	XP_016860309.1:p.Val29615Phe
XM_017004821.1:c.88840G>T (TTN)	XP_016860310.1:p.Val29614Phe
XM_017004822.1:c.85882G>T (TTN)	XP_016860311.1:p.Val28628Phe
XM_017004823.1:c.67498G>T (TTN)	XP_016860312.1:p.Val22500Phe
XM_024453094.1:c.88993G>T (TTN)	XP_024308862.1:p.Val29665Phe
XM_024453095.1:c.88990G>T (TTN)	XP_024308863.1:p.Val29664Phe
XM_024453096.1:c.88423G>T (TTN)	XP_024308864.1:p.Val29475Phe
XM_024453097.1:c.85765G>T (TTN)	XP_024308865.1:p.Val28589Phe
XM_024453098.1:c.85684G>T (TTN)	XP_024308866.1:p.Val28562Phe
XM_024453099.1:c.67447G>T (TTN)	XP_024308867.1:p.Val22483Phe
XM_024453100.1:c.57301G>T (TTN)	XP_024308868.1:p.Val19101Phe