Canonical Allele Identifier: CA349400217

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178527612-G-T
• MyVariant Identifiers: chr2:g.179392339G>T (hg19) ; chr2:g.178527612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527612G>T , CM000664.2:g.178527612G>T	GRCh38
NC_000002.11:g.179392339G>T , CM000664.1:g.179392339G>T	GRCh37
NC_000002.10:g.179100585G>T	NCBI36
NG_011618.3:g.308191C>A , LRG_391:g.308191C>A
NG_051363.1:g.9786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99810C>A (TTN)	ENSP00000343764.6:p.Ser33270Arg
ENST00000342175.11:c.80895C>A (TTN)	ENSP00000340554.6:p.Ser26965Arg
ENST00000359218.10:c.80694C>A (TTN)	ENSP00000352154.5:p.Ser26898Arg
ENST00000342175.10:c.80895C>A (TTN)	ENSP00000340554.6:p.Ser26965Arg
ENST00000342992.10:c.99810C>A (TTN)	ENSP00000343764.6:p.Ser33270Arg
ENST00000359218.9:c.80694C>A (TTN)	ENSP00000352154.5:p.Ser26898Arg
ENST00000460472.6:c.80319C>A (TTN)	ENSP00000434586.1:p.Ser26773Arg
ENST00000589042.5:c.107514C>A (TTN) MANE Select	ENSP00000467141.1:p.Ser35838Arg
ENST00000591111.5:c.102591C>A (TTN)	ENSP00000465570.1:p.Ser34197Arg
ENST00000615779.4:c.102591C>A (TTN)	ENSP00000483597.1:p.Ser34197Arg
NM_001256850.1:c.102591C>A (TTN)	NP_001243779.1:p.Ser34197Arg
NM_001267550.2:c.107514C>A (TTN) MANE Select	NP_001254479.2:p.Ser35838Arg
NM_003319.4:c.80319C>A (TTN)	NP_003310.4:p.Ser26773Arg
NM_133378.4:c.99810C>A (TTN)	NP_596869.4:p.Ser33270Arg
NM_133432.3:c.80694C>A (TTN)	NP_597676.3:p.Ser26898Arg
NM_133437.4:c.80895C>A (TTN)	NP_597681.4:p.Ser26965Arg
NR_038271.1:n.446+3976G>T (TTN-AS1)
NR_038272.1:n.219+3976G>T (TTN-AS1)
XM_011511729.1:c.106611C>A (TTN)	XP_011510031.1:p.Ser35537Arg
XM_011511730.1:c.80505C>A (TTN)	XP_011510032.1:p.Ser26835Arg
XM_011511731.1:c.80364C>A (TTN)	XP_011510033.1:p.Ser26788Arg
XM_017004819.1:c.106407C>A (TTN)	XP_016860308.1:p.Ser35469Arg
XM_017004820.1:c.101805C>A (TTN)	XP_016860309.1:p.Ser33935Arg
XM_017004821.1:c.101802C>A (TTN)	XP_016860310.1:p.Ser33934Arg
XM_017004822.1:c.98844C>A (TTN)	XP_016860311.1:p.Ser32948Arg
XM_017004823.1:c.80460C>A (TTN)	XP_016860312.1:p.Ser26820Arg
XM_024453094.1:c.101955C>A (TTN)	XP_024308862.1:p.Ser33985Arg
XM_024453095.1:c.101952C>A (TTN)	XP_024308863.1:p.Ser33984Arg
XM_024453096.1:c.101385C>A (TTN)	XP_024308864.1:p.Ser33795Arg
XM_024453097.1:c.98727C>A (TTN)	XP_024308865.1:p.Ser32909Arg
XM_024453098.1:c.98646C>A (TTN)	XP_024308866.1:p.Ser32882Arg
XM_024453099.1:c.80409C>A (TTN)	XP_024308867.1:p.Ser26803Arg
XM_024453100.1:c.70263C>A (TTN)	XP_024308868.1:p.Ser23421Arg