Canonical Allele Identifier: CA395176161

Gene: TNRC6A

Linked Data

• gnomAD v4: 16-24793547-C-G
• MyVariant Identifiers: chr16:g.24804868C>G (hg19) ; chr16:g.24793547C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793547C>G , CM000678.2:g.24793547C>G	GRCh38
NC_000016.9:g.24804868C>G , CM000678.1:g.24804868C>G	GRCh37
NC_000016.8:g.24712369C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3250C>G MANE Select	ENSP00000379144.3:p.Pro1084Ala
ENST00000315183.11:c.3250C>G	ENSP00000326900.7:p.Pro1084Ala
ENST00000395799.7:c.3250C>G	ENSP00000379144.3:p.Pro1084Ala
ENST00000450465.6:c.332-997C>G	ENSP00000404278.2:n.332-997C>G
ENST00000491718.5:c.2897C>G
ENST00000567232.1:n.198C>G
ENST00000568903.5:n.203C>G
NM_014494.2:c.3250C>G	NP_055309.2:p.Pro1084Ala
XM_005255254.2:c.3250C>G	XP_005255311.1:p.Pro1084Ala
XM_005255257.3:c.2491C>G	XP_005255314.1:p.Pro831Ala
XM_006721039.2:c.2824C>G	XP_006721102.1:p.Pro942Ala
XM_011545791.1:c.3250C>G	XP_011544093.1:p.Pro1084Ala
XM_011545792.1:c.3250C>G	XP_011544094.1:p.Pro1084Ala
XM_011545793.1:c.3176-997C>G	XP_011544095.1:n.3176-997C>G
XM_011545794.1:c.3176-997C>G	XP_011544096.1:n.3176-997C>G
XM_011545795.1:c.3250C>G	XP_011544097.1:p.Pro1084Ala
XM_011545796.1:c.3250C>G	XP_011544098.1:p.Pro1084Ala
NM_001330520.2:c.3250C>G	NP_001317449.1:p.Pro1084Ala
NM_001351850.1:c.3277C>G	NP_001338779.1:p.Pro1093Ala
NM_014494.3:c.3250C>G	NP_055309.2:p.Pro1084Ala
XM_005255257.4:c.2491C>G	XP_005255314.1:p.Pro831Ala
XM_017023144.2:c.3277C>G	XP_016878633.1:p.Pro1093Ala
XM_017023145.2:c.3277C>G	XP_016878634.1:p.Pro1093Ala
XM_017023146.1:c.3202C>G	XP_016878635.1:p.Pro1068Ala
XM_017023148.2:c.3203-997C>G	XP_016878637.1:n.3203-997C>G
XM_017023150.2:c.3277C>G	XP_016878639.1:p.Pro1093Ala
XM_017023152.2:c.2851C>G	XP_016878641.1:p.Pro951Ala
XM_017023153.1:c.2491C>G	XP_016878642.1:p.Pro831Ala
XM_017023154.1:c.2491C>G	XP_016878643.1:p.Pro831Ala
XM_024450231.1:c.3277C>G	XP_024305999.1:p.Pro1093Ala
XM_024450232.1:c.3277C>G	XP_024306000.1:p.Pro1093Ala
XM_024450233.1:c.3203-997C>G	XP_024306001.1:n.3203-997C>G
NM_014494.4:c.3250C>G MANE Select	NP_055309.2:p.Pro1084Ala
NM_001330520.3:c.3250C>G	NP_001317449.1:p.Pro1084Ala
NM_001351850.2:c.3277C>G	NP_001338779.1:p.Pro1093Ala