Canonical Allele Identifier: CA395176631

Gene: TNRC6A

Linked Data

• MyVariant Identifiers: chr16:g.24804967T>A (hg19) ; chr16:g.24793646T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793646T>A , CM000678.2:g.24793646T>A	GRCh38
NC_000016.9:g.24804967T>A , CM000678.1:g.24804967T>A	GRCh37
NC_000016.8:g.24712468T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3349T>A MANE Select	ENSP00000379144.3:p.Ser1117Thr
ENST00000315183.11:c.3349T>A	ENSP00000326900.7:p.Ser1117Thr
ENST00000395799.7:c.3349T>A	ENSP00000379144.3:p.Ser1117Thr
ENST00000450465.6:c.332-898T>A	ENSP00000404278.2:n.332-898T>A
ENST00000491718.5:c.2996T>A
ENST00000567232.1:n.297T>A
ENST00000568903.5:n.302T>A
NM_014494.2:c.3349T>A	NP_055309.2:p.Ser1117Thr
XM_005255254.2:c.3349T>A	XP_005255311.1:p.Ser1117Thr
XM_005255257.3:c.2590T>A	XP_005255314.1:p.Ser864Thr
XM_006721039.2:c.2923T>A	XP_006721102.1:p.Ser975Thr
XM_011545791.1:c.3349T>A	XP_011544093.1:p.Ser1117Thr
XM_011545792.1:c.3349T>A	XP_011544094.1:p.Ser1117Thr
XM_011545793.1:c.3176-898T>A	XP_011544095.1:n.3176-898T>A
XM_011545794.1:c.3176-898T>A	XP_011544096.1:n.3176-898T>A
XM_011545795.1:c.3349T>A	XP_011544097.1:p.Ser1117Thr
XM_011545796.1:c.3349T>A	XP_011544098.1:p.Ser1117Thr
NM_001330520.2:c.3349T>A	NP_001317449.1:p.Ser1117Thr
NM_001351850.1:c.3376T>A	NP_001338779.1:p.Ser1126Thr
NM_014494.3:c.3349T>A	NP_055309.2:p.Ser1117Thr
XM_005255257.4:c.2590T>A	XP_005255314.1:p.Ser864Thr
XM_017023144.2:c.3376T>A	XP_016878633.1:p.Ser1126Thr
XM_017023145.2:c.3376T>A	XP_016878634.1:p.Ser1126Thr
XM_017023146.1:c.3301T>A	XP_016878635.1:p.Ser1101Thr
XM_017023148.2:c.3203-898T>A	XP_016878637.1:n.3203-898T>A
XM_017023150.2:c.3376T>A	XP_016878639.1:p.Ser1126Thr
XM_017023152.2:c.2950T>A	XP_016878641.1:p.Ser984Thr
XM_017023153.1:c.2590T>A	XP_016878642.1:p.Ser864Thr
XM_017023154.1:c.2590T>A	XP_016878643.1:p.Ser864Thr
XM_024450231.1:c.3376T>A	XP_024305999.1:p.Ser1126Thr
XM_024450232.1:c.3376T>A	XP_024306000.1:p.Ser1126Thr
XM_024450233.1:c.3203-898T>A	XP_024306001.1:n.3203-898T>A
NM_014494.4:c.3349T>A MANE Select	NP_055309.2:p.Ser1117Thr
NM_001330520.3:c.3349T>A	NP_001317449.1:p.Ser1117Thr
NM_001351850.2:c.3376T>A	NP_001338779.1:p.Ser1126Thr