Canonical Allele Identifier: CA349407103

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395273A>T (hg19) ; chr2:g.178530546A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530546A>T , CM000664.2:g.178530546A>T	GRCh38
NC_000002.11:g.179395273A>T , CM000664.1:g.179395273A>T	GRCh37
NC_000002.10:g.179103519A>T	NCBI36
NG_011618.3:g.305257T>A , LRG_391:g.305257T>A
NG_051363.1:g.12720A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98365T>A (TTN)	ENSP00000343764.6:p.Tyr32789Asn
ENST00000342175.11:c.79450T>A (TTN)	ENSP00000340554.6:p.Tyr26484Asn
ENST00000359218.10:c.79249T>A (TTN)	ENSP00000352154.5:p.Tyr26417Asn
ENST00000342175.10:c.79450T>A (TTN)	ENSP00000340554.6:p.Tyr26484Asn
ENST00000342992.10:c.98365T>A (TTN)	ENSP00000343764.6:p.Tyr32789Asn
ENST00000359218.9:c.79249T>A (TTN)	ENSP00000352154.5:p.Tyr26417Asn
ENST00000460472.6:c.78874T>A (TTN)	ENSP00000434586.1:p.Tyr26292Asn
ENST00000589042.5:c.106069T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr35357Asn
ENST00000591111.5:c.101146T>A (TTN)	ENSP00000465570.1:p.Tyr33716Asn
ENST00000615779.4:c.101146T>A (TTN)	ENSP00000483597.1:p.Tyr33716Asn
NM_001256850.1:c.101146T>A (TTN)	NP_001243779.1:p.Tyr33716Asn
NM_001267550.2:c.106069T>A (TTN) MANE Select	NP_001254479.2:p.Tyr35357Asn
NM_003319.4:c.78874T>A (TTN)	NP_003310.4:p.Tyr26292Asn
NM_133378.4:c.98365T>A (TTN)	NP_596869.4:p.Tyr32789Asn
NM_133432.3:c.79249T>A (TTN)	NP_597676.3:p.Tyr26417Asn
NM_133437.4:c.79450T>A (TTN)	NP_597681.4:p.Tyr26484Asn
NR_038271.1:n.446+6910A>T (TTN-AS1)
NR_038272.1:n.220-5186A>T (TTN-AS1)
XM_011511729.1:c.105166T>A (TTN)	XP_011510031.1:p.Tyr35056Asn
XM_011511730.1:c.79060T>A (TTN)	XP_011510032.1:p.Tyr26354Asn
XM_011511731.1:c.78919T>A (TTN)	XP_011510033.1:p.Tyr26307Asn
XM_017004819.1:c.104962T>A (TTN)	XP_016860308.1:p.Tyr34988Asn
XM_017004820.1:c.100360T>A (TTN)	XP_016860309.1:p.Tyr33454Asn
XM_017004821.1:c.100357T>A (TTN)	XP_016860310.1:p.Tyr33453Asn
XM_017004822.1:c.97399T>A (TTN)	XP_016860311.1:p.Tyr32467Asn
XM_017004823.1:c.79015T>A (TTN)	XP_016860312.1:p.Tyr26339Asn
XM_024453094.1:c.100510T>A (TTN)	XP_024308862.1:p.Tyr33504Asn
XM_024453095.1:c.100507T>A (TTN)	XP_024308863.1:p.Tyr33503Asn
XM_024453096.1:c.99940T>A (TTN)	XP_024308864.1:p.Tyr33314Asn
XM_024453097.1:c.97282T>A (TTN)	XP_024308865.1:p.Tyr32428Asn
XM_024453098.1:c.97201T>A (TTN)	XP_024308866.1:p.Tyr32401Asn
XM_024453099.1:c.78964T>A (TTN)	XP_024308867.1:p.Tyr26322Asn
XM_024453100.1:c.68818T>A (TTN)	XP_024308868.1:p.Tyr22940Asn