Canonical Allele Identifier: CA2632373503

Gene: TNRC6A

Linked Data

• gnomAD v4: 16-24793485-CCTGGGGGGAGCCTTCTACTCCAGCCACAACTGTGGATAATGGTACTTCAGCATGGGGTAAGCCCATAGACAGTGGTCCCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793495_24793575del , CM000678.2:g.24793495_24793575del	GRCh38
NC_000016.9:g.24804816_24804896del , CM000678.1:g.24804816_24804896del	GRCh37
NC_000016.8:g.24712317_24712397del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3198_3278del MANE Select	ENSP00000379144.3:p.Pro1067_Glu1093del
ENST00000315183.11:c.3198_3278del	ENSP00000326900.7:p.Pro1067_Glu1093del
ENST00000395799.7:c.3198_3278del	ENSP00000379144.3:p.Pro1067_Glu1093del
ENST00000450465.6:c.332-1049_332-969del	ENSP00000404278.2:n.332-1049_332-969del
ENST00000491718.5:c.2845_2925del
ENST00000567232.1:n.146_226del
ENST00000568903.5:n.151_231del
NM_014494.2:c.3198_3278del	NP_055309.2:p.Pro1067_Glu1093del
XM_005255254.2:c.3198_3278del	XP_005255311.1:p.Pro1067_Glu1093del
XM_005255257.3:c.2439_2519del	XP_005255314.1:p.Pro814_Glu840del
XM_006721039.2:c.2772_2852del	XP_006721102.1:p.Pro925_Glu951del
XM_011545791.1:c.3198_3278del	XP_011544093.1:p.Pro1067_Glu1093del
XM_011545792.1:c.3198_3278del	XP_011544094.1:p.Pro1067_Glu1093del
XM_011545793.1:c.3176-1049_3176-969del	XP_011544095.1:n.3176-1049_3176-969del
XM_011545794.1:c.3176-1049_3176-969del	XP_011544096.1:n.3176-1049_3176-969del
XM_011545795.1:c.3198_3278del	XP_011544097.1:p.Pro1067_Glu1093del
XM_011545796.1:c.3198_3278del	XP_011544098.1:p.Pro1067_Glu1093del
NM_001330520.2:c.3198_3278del	NP_001317449.1:p.Pro1067_Glu1093del
NM_001351850.1:c.3225_3305del	NP_001338779.1:p.Pro1076_Glu1102del
NM_014494.3:c.3198_3278del	NP_055309.2:p.Pro1067_Glu1093del
XM_005255257.4:c.2439_2519del	XP_005255314.1:p.Pro814_Glu840del
XM_017023144.2:c.3225_3305del	XP_016878633.1:p.Pro1076_Glu1102del
XM_017023145.2:c.3225_3305del	XP_016878634.1:p.Pro1076_Glu1102del
XM_017023146.1:c.3150_3230del	XP_016878635.1:p.Pro1051_Glu1077del
XM_017023148.2:c.3203-1049_3203-969del	XP_016878637.1:n.3203-1049_3203-969del
XM_017023150.2:c.3225_3305del	XP_016878639.1:p.Pro1076_Glu1102del
XM_017023152.2:c.2799_2879del	XP_016878641.1:p.Pro934_Glu960del
XM_017023153.1:c.2439_2519del	XP_016878642.1:p.Pro814_Glu840del
XM_017023154.1:c.2439_2519del	XP_016878643.1:p.Pro814_Glu840del
XM_024450231.1:c.3225_3305del	XP_024305999.1:p.Pro1076_Glu1102del
XM_024450232.1:c.3225_3305del	XP_024306000.1:p.Pro1076_Glu1102del
XM_024450233.1:c.3203-1049_3203-969del	XP_024306001.1:n.3203-1049_3203-969del
NM_014494.4:c.3198_3278del MANE Select	NP_055309.2:p.Pro1067_Glu1093del
NM_001330520.3:c.3198_3278del	NP_001317449.1:p.Pro1067_Glu1093del
NM_001351850.2:c.3225_3305del	NP_001338779.1:p.Pro1076_Glu1102del