Canonical Allele Identifier: CA2213968671

Gene: TNRC6A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793761_24793762delinsTG , CM000678.2:g.24793761_24793762delinsTG	GRCh38
NC_000016.9:g.24805082_24805083delinsTG , CM000678.1:g.24805082_24805083delinsTG	GRCh37
NC_000016.8:g.24712583_24712584delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3352+112_3352+113delinsTG MANE Select	ENSP00000379144.3:n.3352+112_3352+113delinsTG
ENST00000315183.11:c.3352+112_3352+113delinsTG	ENSP00000326900.7:n.3352+112_3352+113delinsTG
ENST00000395799.7:c.3352+112_3352+113delinsTG	ENSP00000379144.3:n.3352+112_3352+113delinsTG
ENST00000450465.6:c.332-783_332-782delinsTG	ENSP00000404278.2:n.332-783_332-782delinsTG
ENST00000491718.5:c.2999+112_2999+113delinsTG
ENST00000567232.1:n.300+112_300+113delinsTG
ENST00000568903.5:n.305+112_305+113delinsTG
NM_014494.2:c.3352+112_3352+113delinsTG	NP_055309.2:n.3352+112_3352+113delinsTG
XM_005255254.2:c.3352+112_3352+113delinsTG	XP_005255311.1:n.3352+112_3352+113delinsTG
XM_005255257.3:c.2593+112_2593+113delinsTG	XP_005255314.1:n.2593+112_2593+113delinsTG
XM_006721039.2:c.2926+112_2926+113delinsTG	XP_006721102.1:n.2926+112_2926+113delinsTG
XM_011545791.1:c.3352+112_3352+113delinsTG	XP_011544093.1:n.3352+112_3352+113delinsTG
XM_011545792.1:c.3352+112_3352+113delinsTG	XP_011544094.1:n.3352+112_3352+113delinsTG
XM_011545793.1:c.3176-783_3176-782delinsTG	XP_011544095.1:n.3176-783_3176-782delinsTG
XM_011545794.1:c.3176-783_3176-782delinsTG	XP_011544096.1:n.3176-783_3176-782delinsTG
XM_011545795.1:c.3352+112_3352+113delinsTG	XP_011544097.1:n.3352+112_3352+113delinsTG
XM_011545796.1:c.3352+112_3352+113delinsTG	XP_011544098.1:n.3352+112_3352+113delinsTG
NM_001330520.2:c.3352+112_3352+113delinsTG	NP_001317449.1:n.3352+112_3352+113delinsTG
NM_001351850.1:c.3379+112_3379+113delinsTG	NP_001338779.1:n.3379+112_3379+113delinsTG
NM_014494.3:c.3352+112_3352+113delinsTG	NP_055309.2:n.3352+112_3352+113delinsTG
XM_005255257.4:c.2593+112_2593+113delinsTG	XP_005255314.1:n.2593+112_2593+113delinsTG
XM_017023144.2:c.3379+112_3379+113delinsTG	XP_016878633.1:n.3379+112_3379+113delinsTG
XM_017023145.2:c.3379+112_3379+113delinsTG	XP_016878634.1:n.3379+112_3379+113delinsTG
XM_017023146.1:c.3304+112_3304+113delinsTG	XP_016878635.1:n.3304+112_3304+113delinsTG
XM_017023148.2:c.3203-783_3203-782delinsTG	XP_016878637.1:n.3203-783_3203-782delinsTG
XM_017023150.2:c.3379+112_3379+113delinsTG	XP_016878639.1:n.3379+112_3379+113delinsTG
XM_017023152.2:c.2953+112_2953+113delinsTG	XP_016878641.1:n.2953+112_2953+113delinsTG
XM_017023153.1:c.2593+112_2593+113delinsTG	XP_016878642.1:n.2593+112_2593+113delinsTG
XM_017023154.1:c.2593+112_2593+113delinsTG	XP_016878643.1:n.2593+112_2593+113delinsTG
XM_024450231.1:c.3379+112_3379+113delinsTG	XP_024305999.1:n.3379+112_3379+113delinsTG
XM_024450232.1:c.3379+112_3379+113delinsTG	XP_024306000.1:n.3379+112_3379+113delinsTG
XM_024450233.1:c.3203-783_3203-782delinsTG	XP_024306001.1:n.3203-783_3203-782delinsTG
NM_014494.4:c.3352+112_3352+113delinsTG MANE Select	NP_055309.2:n.3352+112_3352+113delinsTG
NM_001330520.3:c.3352+112_3352+113delinsTG	NP_001317449.1:n.3352+112_3352+113delinsTG
NM_001351850.2:c.3379+112_3379+113delinsTG	NP_001338779.1:n.3379+112_3379+113delinsTG