Canonical Allele Identifier: CA761291853

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1303380832
• gnomAD v3: 2-178581425-A-G
• gnomAD v4: 2-178581425-A-G
• MyVariant Identifiers: chr2:g.179446152A>G (hg19) ; chr2:g.178581425A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178581425A>G , CM000664.2:g.178581425A>G	GRCh38
NC_000002.11:g.179446152A>G , CM000664.1:g.179446152A>G	GRCh37
NC_000002.10:g.179154398A>G	NCBI36
NG_011618.3:g.254378T>C , LRG_391:g.254378T>C
NG_051363.1:g.63599A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.59065+74T>C (TTN)	ENSP00000343764.6:n.59065+74T>C
ENST00000342175.11:c.40150+74T>C (TTN)	ENSP00000340554.6:n.40150+74T>C
ENST00000359218.10:c.39949+74T>C (TTN)	ENSP00000352154.5:n.39949+74T>C
ENST00000342175.10:c.40150+74T>C (TTN)	ENSP00000340554.6:n.40150+74T>C
ENST00000342992.10:c.59065+74T>C (TTN)	ENSP00000343764.6:n.59065+74T>C
ENST00000359218.9:c.39949+74T>C (TTN)	ENSP00000352154.5:n.39949+74T>C
ENST00000460472.6:c.39574+74T>C (TTN)	ENSP00000434586.1:n.39574+74T>C
ENST00000589042.5:c.66769+74T>C (TTN) MANE Select	ENSP00000467141.1:n.66769+74T>C
ENST00000591111.5:c.61846+74T>C (TTN)	ENSP00000465570.1:n.61846+74T>C
ENST00000615779.4:c.61846+74T>C (TTN)	ENSP00000483597.1:n.61846+74T>C
NM_001256850.1:c.61846+74T>C (TTN)	NP_001243779.1:n.61846+74T>C
NM_001267550.2:c.66769+74T>C (TTN) MANE Select	NP_001254479.2:n.66769+74T>C
NM_003319.4:c.39574+74T>C (TTN)	NP_003310.4:n.39574+74T>C
NM_133378.4:c.59065+74T>C (TTN)	NP_596869.4:n.59065+74T>C
NM_133432.3:c.39949+74T>C (TTN)	NP_597676.3:n.39949+74T>C
NM_133437.4:c.40150+74T>C (TTN)	NP_597681.4:n.40150+74T>C
NR_038271.1:n.596+9976A>G (TTN-AS1)
NR_038272.1:n.2044-1147A>G (TTN-AS1)
XM_011511729.1:c.65866+74T>C (TTN)	XP_011510031.1:n.65866+74T>C
XM_011511730.1:c.39760+74T>C (TTN)	XP_011510032.1:n.39760+74T>C
XM_011511731.1:c.39619+74T>C (TTN)	XP_011510033.1:n.39619+74T>C
XM_017004819.1:c.65662+74T>C (TTN)	XP_016860308.1:n.65662+74T>C
XM_017004820.1:c.61060+74T>C (TTN)	XP_016860309.1:n.61060+74T>C
XM_017004821.1:c.61057+74T>C (TTN)	XP_016860310.1:n.61057+74T>C
XM_017004822.1:c.58099+74T>C (TTN)	XP_016860311.1:n.58099+74T>C
XM_017004823.1:c.39715+74T>C (TTN)	XP_016860312.1:n.39715+74T>C
XM_024453094.1:c.61210+74T>C (TTN)	XP_024308862.1:n.61210+74T>C
XM_024453095.1:c.61207+74T>C (TTN)	XP_024308863.1:n.61207+74T>C
XM_024453096.1:c.60640+74T>C (TTN)	XP_024308864.1:n.60640+74T>C
XM_024453097.1:c.57982+74T>C (TTN)	XP_024308865.1:n.57982+74T>C
XM_024453098.1:c.57901+74T>C (TTN)	XP_024308866.1:n.57901+74T>C
XM_024453099.1:c.39664+74T>C (TTN)	XP_024308867.1:n.39664+74T>C
XM_024453100.1:c.29518+74T>C (TTN)	XP_024308868.1:n.29518+74T>C