Canonical Allele Identifier: CA761305818

Gene: TTN

Linked Data

• dbSNP Id: rs1233723518
• MyVariant Identifiers: chr2:g.179577398_179577399insG (hg19) ; chr2:g.178712671_178712672insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178712671_178712672insG , CM000664.2:g.178712671_178712672insG	GRCh38
NC_000002.11:g.179577398_179577399insG , CM000664.1:g.179577398_179577399insG	GRCh37
NC_000002.10:g.179285643_179285644insG	NCBI36
NG_011618.3:g.123131_123132insC , LRG_391:g.123131_123132insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.23596+25_23596+26insC	ENSP00000343764.6:n.23596+25_23596+26insC
ENST00000342175.11:c.13858+25410_13858+25411insC	ENSP00000340554.6:n.13858+25410_13858+25411insC
ENST00000359218.10:c.13657+25410_13657+25411insC	ENSP00000352154.5:n.13657+25410_13657+25411insC
ENST00000342175.10:c.13858+25410_13858+25411insC	ENSP00000340554.6:n.13858+25410_13858+25411insC
ENST00000342992.10:c.23596+25_23596+26insC	ENSP00000343764.6:n.23596+25_23596+26insC
ENST00000359218.9:c.13657+25410_13657+25411insC	ENSP00000352154.5:n.13657+25410_13657+25411insC
ENST00000460472.6:c.13282+25410_13282+25411insC	ENSP00000434586.1:n.13282+25410_13282+25411insC
ENST00000589042.5:c.27328+25_27328+26insC MANE Select	ENSP00000467141.1:n.27328+25_27328+26insC
ENST00000591111.5:c.26377+25_26377+26insC	ENSP00000465570.1:n.26377+25_26377+26insC
ENST00000615779.4:c.26377+25_26377+26insC	ENSP00000483597.1:n.26377+25_26377+26insC
NM_001256850.1:c.26377+25_26377+26insC	NP_001243779.1:n.26377+25_26377+26insC
NM_001267550.2:c.27328+25_27328+26insC MANE Select	NP_001254479.2:n.27328+25_27328+26insC
NM_003319.4:c.13282+25410_13282+25411insC	NP_003310.4:n.13282+25410_13282+25411insC
NM_133378.4:c.23596+25_23596+26insC	NP_596869.4:n.23596+25_23596+26insC
NM_133432.3:c.13657+25410_13657+25411insC	NP_597676.3:n.13657+25410_13657+25411insC
NM_133437.4:c.13858+25410_13858+25411insC	NP_597681.4:n.13858+25410_13858+25411insC
XM_011511729.1:c.26425+25_26425+26insC	XP_011510031.1:n.26425+25_26425+26insC
XM_011511730.1:c.13468+25410_13468+25411insC	XP_011510032.1:n.13468+25410_13468+25411insC
XM_011511731.1:c.13327+25410_13327+25411insC	XP_011510033.1:n.13327+25410_13327+25411insC
XM_017004819.1:c.26380+25_26380+26insC	XP_016860308.1:n.26380+25_26380+26insC
XM_017004820.1:c.23599+25_23599+26insC	XP_016860309.1:n.23599+25_23599+26insC
XM_017004821.1:c.23596+25_23596+26insC	XP_016860310.1:n.23596+25_23596+26insC
XM_017004822.1:c.26380+25_26380+26insC	XP_016860311.1:n.26380+25_26380+26insC
XM_017004823.1:c.13423+25410_13423+25411insC	XP_016860312.1:n.13423+25410_13423+25411insC
XM_024453094.1:c.26380+25_26380+26insC	XP_024308862.1:n.26380+25_26380+26insC
XM_024453095.1:c.26380+25_26380+26insC	XP_024308863.1:n.26380+25_26380+26insC
XM_024453096.1:c.26380+25_26380+26insC	XP_024308864.1:n.26380+25_26380+26insC
XM_024453097.1:c.26380+25_26380+26insC	XP_024308865.1:n.26380+25_26380+26insC
XM_024453098.1:c.26380+25_26380+26insC	XP_024308866.1:n.26380+25_26380+26insC
XM_024453099.1:c.13423+25410_13423+25411insC	XP_024308867.1:n.13423+25410_13423+25411insC