Canonical Allele Identifier: CA2662134742

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178618224-TCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618227_178618229del , CM000664.2:g.178618227_178618229del	GRCh38
NC_000002.11:g.179482954_179482956del , CM000664.1:g.179482954_179482956del	GRCh37
NC_000002.10:g.179191199_179191201del	NCBI36
NG_011618.3:g.217576_217578del , LRG_391:g.217576_217578del
NG_051363.1:g.100401_100403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39527_39529del (TTN)	ENSP00000343764.6:p.Val13176del
ENST00000342175.11:c.20612_20614del (TTN)	ENSP00000340554.6:p.Val6871del
ENST00000359218.10:c.20411_20413del (TTN)	ENSP00000352154.5:p.Val6804del
ENST00000342175.10:c.20612_20614del (TTN)	ENSP00000340554.6:p.Val6871del
ENST00000342992.10:c.39527_39529del (TTN)	ENSP00000343764.6:p.Val13176del
ENST00000359218.9:c.20411_20413del (TTN)	ENSP00000352154.5:p.Val6804del
ENST00000460472.6:c.20036_20038del (TTN)	ENSP00000434586.1:p.Val6679del
ENST00000589042.5:c.47231_47233del (TTN) MANE Select	ENSP00000467141.1:p.Val15744del
ENST00000591111.5:c.42308_42310del (TTN)	ENSP00000465570.1:p.Val14103del
ENST00000615779.4:c.42308_42310del (TTN)	ENSP00000483597.1:p.Val14103del
NM_001256850.1:c.42308_42310del (TTN)	NP_001243779.1:p.Val14103del
NM_001267550.2:c.47231_47233del (TTN) MANE Select	NP_001254479.2:p.Val15744del
NM_003319.4:c.20036_20038del (TTN)	NP_003310.4:p.Val6679del
NM_133378.4:c.39527_39529del (TTN)	NP_596869.4:p.Val13176del
NM_133432.3:c.20411_20413del (TTN)	NP_597676.3:p.Val6804del
NM_133437.4:c.20612_20614del (TTN)	NP_597681.4:p.Val6871del
NR_038271.1:n.1605-1526_1605-1524del (TTN-AS1)
XM_011511729.1:c.46328_46330del (TTN)	XP_011510031.1:p.Val15443del
XM_011511730.1:c.20222_20224del (TTN)	XP_011510032.1:p.Val6741del
XM_011511731.1:c.20081_20083del (TTN)	XP_011510033.1:p.Val6694del
XM_017004819.1:c.46124_46126del (TTN)	XP_016860308.1:p.Val15375del
XM_017004820.1:c.41522_41524del (TTN)	XP_016860309.1:p.Val13841del
XM_017004821.1:c.41519_41521del (TTN)	XP_016860310.1:p.Val13840del
XM_017004822.1:c.38561_38563del (TTN)	XP_016860311.1:p.Val12854del
XM_017004823.1:c.20177_20179del (TTN)	XP_016860312.1:p.Val6726del
XM_024453094.1:c.41672_41674del (TTN)	XP_024308862.1:p.Val13891del
XM_024453095.1:c.41669_41671del (TTN)	XP_024308863.1:p.Val13890del
XM_024453096.1:c.41102_41104del (TTN)	XP_024308864.1:p.Val13701del
XM_024453097.1:c.38444_38446del (TTN)	XP_024308865.1:p.Val12815del
XM_024453098.1:c.38363_38365del (TTN)	XP_024308866.1:p.Val12788del
XM_024453099.1:c.20126_20128del (TTN)	XP_024308867.1:p.Val6709del
XM_024453100.1:c.9980_9982del (TTN)	XP_024308868.1:p.Val3327del