Canonical Allele Identifier: CA349405206

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394762C>T (hg19) ; chr2:g.178530035C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530035C>T , CM000664.2:g.178530035C>T	GRCh38
NC_000002.11:g.179394762C>T , CM000664.1:g.179394762C>T	GRCh37
NC_000002.10:g.179103008C>T	NCBI36
NG_011618.3:g.305768G>A , LRG_391:g.305768G>A
NG_051363.1:g.12209C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98752G>A (TTN)	ENSP00000343764.6:p.Asp32918Asn
ENST00000342175.11:c.79837G>A (TTN)	ENSP00000340554.6:p.Asp26613Asn
ENST00000359218.10:c.79636G>A (TTN)	ENSP00000352154.5:p.Asp26546Asn
ENST00000342175.10:c.79837G>A (TTN)	ENSP00000340554.6:p.Asp26613Asn
ENST00000342992.10:c.98752G>A (TTN)	ENSP00000343764.6:p.Asp32918Asn
ENST00000359218.9:c.79636G>A (TTN)	ENSP00000352154.5:p.Asp26546Asn
ENST00000460472.6:c.79261G>A (TTN)	ENSP00000434586.1:p.Asp26421Asn
ENST00000589042.5:c.106456G>A (TTN) MANE Select	ENSP00000467141.1:p.Asp35486Asn
ENST00000591111.5:c.101533G>A (TTN)	ENSP00000465570.1:p.Asp33845Asn
ENST00000615779.4:c.101533G>A (TTN)	ENSP00000483597.1:p.Asp33845Asn
NM_001256850.1:c.101533G>A (TTN)	NP_001243779.1:p.Asp33845Asn
NM_001267550.2:c.106456G>A (TTN) MANE Select	NP_001254479.2:p.Asp35486Asn
NM_003319.4:c.79261G>A (TTN)	NP_003310.4:p.Asp26421Asn
NM_133378.4:c.98752G>A (TTN)	NP_596869.4:p.Asp32918Asn
NM_133432.3:c.79636G>A (TTN)	NP_597676.3:p.Asp26546Asn
NM_133437.4:c.79837G>A (TTN)	NP_597681.4:p.Asp26613Asn
NR_038271.1:n.446+6399C>T (TTN-AS1)
NR_038272.1:n.220-5697C>T (TTN-AS1)
XM_011511729.1:c.105553G>A (TTN)	XP_011510031.1:p.Asp35185Asn
XM_011511730.1:c.79447G>A (TTN)	XP_011510032.1:p.Asp26483Asn
XM_011511731.1:c.79306G>A (TTN)	XP_011510033.1:p.Asp26436Asn
XM_017004819.1:c.105349G>A (TTN)	XP_016860308.1:p.Asp35117Asn
XM_017004820.1:c.100747G>A (TTN)	XP_016860309.1:p.Asp33583Asn
XM_017004821.1:c.100744G>A (TTN)	XP_016860310.1:p.Asp33582Asn
XM_017004822.1:c.97786G>A (TTN)	XP_016860311.1:p.Asp32596Asn
XM_017004823.1:c.79402G>A (TTN)	XP_016860312.1:p.Asp26468Asn
XM_024453094.1:c.100897G>A (TTN)	XP_024308862.1:p.Asp33633Asn
XM_024453095.1:c.100894G>A (TTN)	XP_024308863.1:p.Asp33632Asn
XM_024453096.1:c.100327G>A (TTN)	XP_024308864.1:p.Asp33443Asn
XM_024453097.1:c.97669G>A (TTN)	XP_024308865.1:p.Asp32557Asn
XM_024453098.1:c.97588G>A (TTN)	XP_024308866.1:p.Asp32530Asn
XM_024453099.1:c.79351G>A (TTN)	XP_024308867.1:p.Asp26451Asn
XM_024453100.1:c.69205G>A (TTN)	XP_024308868.1:p.Asp23069Asn