Canonical Allele Identifier: CA2213968321

Gene: TNRC6A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793530C= , CM000678.2:g.24793530C=	GRCh38
NC_000016.9:g.24804851C= , CM000678.1:g.24804851C=	GRCh37
NC_000016.8:g.24712352C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3233C= MANE Select	ENSP00000379144.3:p.Thr1078=
ENST00000315183.11:c.3233C=	ENSP00000326900.7:p.Thr1078=
ENST00000395799.7:c.3233C=	ENSP00000379144.3:p.Thr1078=
ENST00000450465.6:c.332-1014C=	ENSP00000404278.2:n.332-1014C=
ENST00000491718.5:c.2880C=
ENST00000567232.1:n.181C=
ENST00000568903.5:n.186C=
NM_014494.2:c.3233C=	NP_055309.2:p.Thr1078=
XM_005255254.2:c.3233C=	XP_005255311.1:p.Thr1078=
XM_005255257.3:c.2474C=	XP_005255314.1:p.Thr825=
XM_006721039.2:c.2807C=	XP_006721102.1:p.Thr936=
XM_011545791.1:c.3233C=	XP_011544093.1:p.Thr1078=
XM_011545792.1:c.3233C=	XP_011544094.1:p.Thr1078=
XM_011545793.1:c.3176-1014C=	XP_011544095.1:n.3176-1014C=
XM_011545794.1:c.3176-1014C=	XP_011544096.1:n.3176-1014C=
XM_011545795.1:c.3233C=	XP_011544097.1:p.Thr1078=
XM_011545796.1:c.3233C=	XP_011544098.1:p.Thr1078=
NM_001330520.2:c.3233C=	NP_001317449.1:p.Thr1078=
NM_001351850.1:c.3260C=	NP_001338779.1:p.Thr1087=
NM_014494.3:c.3233C=	NP_055309.2:p.Thr1078=
XM_005255257.4:c.2474C=	XP_005255314.1:p.Thr825=
XM_017023144.2:c.3260C=	XP_016878633.1:p.Thr1087=
XM_017023145.2:c.3260C=	XP_016878634.1:p.Thr1087=
XM_017023146.1:c.3185C=	XP_016878635.1:p.Thr1062=
XM_017023148.2:c.3203-1014C=	XP_016878637.1:n.3203-1014C=
XM_017023150.2:c.3260C=	XP_016878639.1:p.Thr1087=
XM_017023152.2:c.2834C=	XP_016878641.1:p.Thr945=
XM_017023153.1:c.2474C=	XP_016878642.1:p.Thr825=
XM_017023154.1:c.2474C=	XP_016878643.1:p.Thr825=
XM_024450231.1:c.3260C=	XP_024305999.1:p.Thr1087=
XM_024450232.1:c.3260C=	XP_024306000.1:p.Thr1087=
XM_024450233.1:c.3203-1014C=	XP_024306001.1:n.3203-1014C=
NM_014494.4:c.3233C= MANE Select	NP_055309.2:p.Thr1078=
NM_001330520.3:c.3233C=	NP_001317449.1:p.Thr1078=
NM_001351850.2:c.3260C=	NP_001338779.1:p.Thr1087=