Canonical Allele Identifier: CA349407144

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395293G>T (hg19) ; chr2:g.178530566G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530566G>T , CM000664.2:g.178530566G>T	GRCh38
NC_000002.11:g.179395293G>T , CM000664.1:g.179395293G>T	GRCh37
NC_000002.10:g.179103539G>T	NCBI36
NG_011618.3:g.305237C>A , LRG_391:g.305237C>A
NG_051363.1:g.12740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98345C>A (TTN)	ENSP00000343764.6:p.Thr32782Asn
ENST00000342175.11:c.79430C>A (TTN)	ENSP00000340554.6:p.Thr26477Asn
ENST00000359218.10:c.79229C>A (TTN)	ENSP00000352154.5:p.Thr26410Asn
ENST00000342175.10:c.79430C>A (TTN)	ENSP00000340554.6:p.Thr26477Asn
ENST00000342992.10:c.98345C>A (TTN)	ENSP00000343764.6:p.Thr32782Asn
ENST00000359218.9:c.79229C>A (TTN)	ENSP00000352154.5:p.Thr26410Asn
ENST00000460472.6:c.78854C>A (TTN)	ENSP00000434586.1:p.Thr26285Asn
ENST00000589042.5:c.106049C>A (TTN) MANE Select	ENSP00000467141.1:p.Thr35350Asn
ENST00000591111.5:c.101126C>A (TTN)	ENSP00000465570.1:p.Thr33709Asn
ENST00000615779.4:c.101126C>A (TTN)	ENSP00000483597.1:p.Thr33709Asn
NM_001256850.1:c.101126C>A (TTN)	NP_001243779.1:p.Thr33709Asn
NM_001267550.2:c.106049C>A (TTN) MANE Select	NP_001254479.2:p.Thr35350Asn
NM_003319.4:c.78854C>A (TTN)	NP_003310.4:p.Thr26285Asn
NM_133378.4:c.98345C>A (TTN)	NP_596869.4:p.Thr32782Asn
NM_133432.3:c.79229C>A (TTN)	NP_597676.3:p.Thr26410Asn
NM_133437.4:c.79430C>A (TTN)	NP_597681.4:p.Thr26477Asn
NR_038271.1:n.446+6930G>T (TTN-AS1)
NR_038272.1:n.220-5166G>T (TTN-AS1)
XM_011511729.1:c.105146C>A (TTN)	XP_011510031.1:p.Thr35049Asn
XM_011511730.1:c.79040C>A (TTN)	XP_011510032.1:p.Thr26347Asn
XM_011511731.1:c.78899C>A (TTN)	XP_011510033.1:p.Thr26300Asn
XM_017004819.1:c.104942C>A (TTN)	XP_016860308.1:p.Thr34981Asn
XM_017004820.1:c.100340C>A (TTN)	XP_016860309.1:p.Thr33447Asn
XM_017004821.1:c.100337C>A (TTN)	XP_016860310.1:p.Thr33446Asn
XM_017004822.1:c.97379C>A (TTN)	XP_016860311.1:p.Thr32460Asn
XM_017004823.1:c.78995C>A (TTN)	XP_016860312.1:p.Thr26332Asn
XM_024453094.1:c.100490C>A (TTN)	XP_024308862.1:p.Thr33497Asn
XM_024453095.1:c.100487C>A (TTN)	XP_024308863.1:p.Thr33496Asn
XM_024453096.1:c.99920C>A (TTN)	XP_024308864.1:p.Thr33307Asn
XM_024453097.1:c.97262C>A (TTN)	XP_024308865.1:p.Thr32421Asn
XM_024453098.1:c.97181C>A (TTN)	XP_024308866.1:p.Thr32394Asn
XM_024453099.1:c.78944C>A (TTN)	XP_024308867.1:p.Thr26315Asn
XM_024453100.1:c.68798C>A (TTN)	XP_024308868.1:p.Thr22933Asn