Canonical Allele Identifier: CA494198284
Gene: TNRC6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.24804894G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.24793573G>A , CM000678.2:g.24793573G>A GRCh38
NC_000016.9:g.24804894G>A , CM000678.1:g.24804894G>A GRCh37
NC_000016.8:g.24712395G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395799.8:c.3276G>A MANE Select ENSP00000379144.3:p.Gly1092=
ENST00000315183.11:c.3276G>A ENSP00000326900.7:p.Gly1092=
ENST00000395799.7:c.3276G>A ENSP00000379144.3:p.Gly1092=
ENST00000450465.6:c.332-971G>A ENSP00000404278.2:n.332-971G>A
ENST00000491718.5:c.2923G>A
ENST00000567232.1:n.224G>A
ENST00000568903.5:n.229G>A
NM_014494.2:c.3276G>A NP_055309.2:p.Gly1092=
XM_005255254.2:c.3276G>A XP_005255311.1:p.Gly1092=
XM_005255257.3:c.2517G>A XP_005255314.1:p.Gly839=
XM_006721039.2:c.2850G>A XP_006721102.1:p.Gly950=
XM_011545791.1:c.3276G>A XP_011544093.1:p.Gly1092=
XM_011545792.1:c.3276G>A XP_011544094.1:p.Gly1092=
XM_011545793.1:c.3176-971G>A XP_011544095.1:n.3176-971G>A
XM_011545794.1:c.3176-971G>A XP_011544096.1:n.3176-971G>A
XM_011545795.1:c.3276G>A XP_011544097.1:p.Gly1092=
XM_011545796.1:c.3276G>A XP_011544098.1:p.Gly1092=
NM_001330520.2:c.3276G>A NP_001317449.1:p.Gly1092=
NM_001351850.1:c.3303G>A NP_001338779.1:p.Gly1101=
NM_014494.3:c.3276G>A NP_055309.2:p.Gly1092=
XM_005255257.4:c.2517G>A XP_005255314.1:p.Gly839=
XM_017023144.2:c.3303G>A XP_016878633.1:p.Gly1101=
XM_017023145.2:c.3303G>A XP_016878634.1:p.Gly1101=
XM_017023146.1:c.3228G>A XP_016878635.1:p.Gly1076=
XM_017023148.2:c.3203-971G>A XP_016878637.1:n.3203-971G>A
XM_017023150.2:c.3303G>A XP_016878639.1:p.Gly1101=
XM_017023152.2:c.2877G>A XP_016878641.1:p.Gly959=
XM_017023153.1:c.2517G>A XP_016878642.1:p.Gly839=
XM_017023154.1:c.2517G>A XP_016878643.1:p.Gly839=
XM_024450231.1:c.3303G>A XP_024305999.1:p.Gly1101=
XM_024450232.1:c.3303G>A XP_024306000.1:p.Gly1101=
XM_024450233.1:c.3203-971G>A XP_024306001.1:n.3203-971G>A
NM_014494.4:c.3276G>A MANE Select NP_055309.2:p.Gly1092=
NM_001330520.3:c.3276G>A NP_001317449.1:p.Gly1092=
NM_001351850.2:c.3303G>A NP_001338779.1:p.Gly1101=