Canonical Allele Identifier: CA395176245

Gene: TNRC6A

Linked Data

• MyVariant Identifiers: chr16:g.24804888C>G (hg19) ; chr16:g.24793567C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793567C>G , CM000678.2:g.24793567C>G	GRCh38
NC_000016.9:g.24804888C>G , CM000678.1:g.24804888C>G	GRCh37
NC_000016.8:g.24712389C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3270C>G MANE Select	ENSP00000379144.3:p.Ser1090Arg
ENST00000315183.11:c.3270C>G	ENSP00000326900.7:p.Ser1090Arg
ENST00000395799.7:c.3270C>G	ENSP00000379144.3:p.Ser1090Arg
ENST00000450465.6:c.332-977C>G	ENSP00000404278.2:n.332-977C>G
ENST00000491718.5:c.2917C>G
ENST00000567232.1:n.218C>G
ENST00000568903.5:n.223C>G
NM_014494.2:c.3270C>G	NP_055309.2:p.Ser1090Arg
XM_005255254.2:c.3270C>G	XP_005255311.1:p.Ser1090Arg
XM_005255257.3:c.2511C>G	XP_005255314.1:p.Ser837Arg
XM_006721039.2:c.2844C>G	XP_006721102.1:p.Ser948Arg
XM_011545791.1:c.3270C>G	XP_011544093.1:p.Ser1090Arg
XM_011545792.1:c.3270C>G	XP_011544094.1:p.Ser1090Arg
XM_011545793.1:c.3176-977C>G	XP_011544095.1:n.3176-977C>G
XM_011545794.1:c.3176-977C>G	XP_011544096.1:n.3176-977C>G
XM_011545795.1:c.3270C>G	XP_011544097.1:p.Ser1090Arg
XM_011545796.1:c.3270C>G	XP_011544098.1:p.Ser1090Arg
NM_001330520.2:c.3270C>G	NP_001317449.1:p.Ser1090Arg
NM_001351850.1:c.3297C>G	NP_001338779.1:p.Ser1099Arg
NM_014494.3:c.3270C>G	NP_055309.2:p.Ser1090Arg
XM_005255257.4:c.2511C>G	XP_005255314.1:p.Ser837Arg
XM_017023144.2:c.3297C>G	XP_016878633.1:p.Ser1099Arg
XM_017023145.2:c.3297C>G	XP_016878634.1:p.Ser1099Arg
XM_017023146.1:c.3222C>G	XP_016878635.1:p.Ser1074Arg
XM_017023148.2:c.3203-977C>G	XP_016878637.1:n.3203-977C>G
XM_017023150.2:c.3297C>G	XP_016878639.1:p.Ser1099Arg
XM_017023152.2:c.2871C>G	XP_016878641.1:p.Ser957Arg
XM_017023153.1:c.2511C>G	XP_016878642.1:p.Ser837Arg
XM_017023154.1:c.2511C>G	XP_016878643.1:p.Ser837Arg
XM_024450231.1:c.3297C>G	XP_024305999.1:p.Ser1099Arg
XM_024450232.1:c.3297C>G	XP_024306000.1:p.Ser1099Arg
XM_024450233.1:c.3203-977C>G	XP_024306001.1:n.3203-977C>G
NM_014494.4:c.3270C>G MANE Select	NP_055309.2:p.Ser1090Arg
NM_001330520.3:c.3270C>G	NP_001317449.1:p.Ser1090Arg
NM_001351850.2:c.3297C>G	NP_001338779.1:p.Ser1099Arg