Canonical Allele Identifier: CA349456913

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409111G>T (hg19) ; chr2:g.178544384G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544384G>T , CM000664.2:g.178544384G>T	GRCh38
NC_000002.11:g.179409111G>T , CM000664.1:g.179409111G>T	GRCh37
NC_000002.10:g.179117357G>T	NCBI36
NG_011618.3:g.291419C>A , LRG_391:g.291419C>A
NG_051363.1:g.26558G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88141C>A (TTN)	ENSP00000343764.6:p.Gln29381Lys
ENST00000342175.11:c.69226C>A (TTN)	ENSP00000340554.6:p.Gln23076Lys
ENST00000359218.10:c.69025C>A (TTN)	ENSP00000352154.5:p.Gln23009Lys
ENST00000342175.10:c.69226C>A (TTN)	ENSP00000340554.6:p.Gln23076Lys
ENST00000342992.10:c.88141C>A (TTN)	ENSP00000343764.6:p.Gln29381Lys
ENST00000359218.9:c.69025C>A (TTN)	ENSP00000352154.5:p.Gln23009Lys
ENST00000460472.6:c.68650C>A (TTN)	ENSP00000434586.1:p.Gln22884Lys
ENST00000589042.5:c.95845C>A (TTN) MANE Select	ENSP00000467141.1:p.Gln31949Lys
ENST00000591111.5:c.90922C>A (TTN)	ENSP00000465570.1:p.Gln30308Lys
ENST00000615779.4:c.90922C>A (TTN)	ENSP00000483597.1:p.Gln30308Lys
NM_001256850.1:c.90922C>A (TTN)	NP_001243779.1:p.Gln30308Lys
NM_001267550.2:c.95845C>A (TTN) MANE Select	NP_001254479.2:p.Gln31949Lys
NM_003319.4:c.68650C>A (TTN)	NP_003310.4:p.Gln22884Lys
NM_133378.4:c.88141C>A (TTN)	NP_596869.4:p.Gln29381Lys
NM_133432.3:c.69025C>A (TTN)	NP_597676.3:p.Gln23009Lys
NM_133437.4:c.69226C>A (TTN)	NP_597681.4:p.Gln23076Lys
NR_038271.1:n.446+20748G>T (TTN-AS1)
NR_038272.1:n.2043+2023G>T (TTN-AS1)
XM_011511729.1:c.94942C>A (TTN)	XP_011510031.1:p.Gln31648Lys
XM_011511730.1:c.68836C>A (TTN)	XP_011510032.1:p.Gln22946Lys
XM_011511731.1:c.68695C>A (TTN)	XP_011510033.1:p.Gln22899Lys
XM_017004819.1:c.94738C>A (TTN)	XP_016860308.1:p.Gln31580Lys
XM_017004820.1:c.90136C>A (TTN)	XP_016860309.1:p.Gln30046Lys
XM_017004821.1:c.90133C>A (TTN)	XP_016860310.1:p.Gln30045Lys
XM_017004822.1:c.87175C>A (TTN)	XP_016860311.1:p.Gln29059Lys
XM_017004823.1:c.68791C>A (TTN)	XP_016860312.1:p.Gln22931Lys
XM_024453094.1:c.90286C>A (TTN)	XP_024308862.1:p.Gln30096Lys
XM_024453095.1:c.90283C>A (TTN)	XP_024308863.1:p.Gln30095Lys
XM_024453096.1:c.89716C>A (TTN)	XP_024308864.1:p.Gln29906Lys
XM_024453097.1:c.87058C>A (TTN)	XP_024308865.1:p.Gln29020Lys
XM_024453098.1:c.86977C>A (TTN)	XP_024308866.1:p.Gln28993Lys
XM_024453099.1:c.68740C>A (TTN)	XP_024308867.1:p.Gln22914Lys
XM_024453100.1:c.58594C>A (TTN)	XP_024308868.1:p.Gln19532Lys