Canonical Allele Identifier: CA7968887

Gene: TNRC6A

Linked Data

• dbSNP Id: rs753592823
• ExAC: 16:24804955 G / C
• gnomAD v2: 16-24804955-G-C
• MyVariant Identifiers: chr16:g.24804955G>C (hg19) ; chr16:g.24793634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.24793634G>C , CM000678.2:g.24793634G>C	GRCh38
NC_000016.9:g.24804955G>C , CM000678.1:g.24804955G>C	GRCh37
NC_000016.8:g.24712456G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395799.8:c.3337G>C MANE Select	ENSP00000379144.3:p.Ala1113Pro
ENST00000315183.11:c.3337G>C	ENSP00000326900.7:p.Ala1113Pro
ENST00000395799.7:c.3337G>C	ENSP00000379144.3:p.Ala1113Pro
ENST00000450465.6:c.332-910G>C	ENSP00000404278.2:n.332-910G>C
ENST00000491718.5:c.2984G>C
ENST00000567232.1:n.285G>C
ENST00000568903.5:n.290G>C
NM_014494.2:c.3337G>C	NP_055309.2:p.Ala1113Pro
XM_005255254.2:c.3337G>C	XP_005255311.1:p.Ala1113Pro
XM_005255257.3:c.2578G>C	XP_005255314.1:p.Ala860Pro
XM_006721039.2:c.2911G>C	XP_006721102.1:p.Ala971Pro
XM_011545791.1:c.3337G>C	XP_011544093.1:p.Ala1113Pro
XM_011545792.1:c.3337G>C	XP_011544094.1:p.Ala1113Pro
XM_011545793.1:c.3176-910G>C	XP_011544095.1:n.3176-910G>C
XM_011545794.1:c.3176-910G>C	XP_011544096.1:n.3176-910G>C
XM_011545795.1:c.3337G>C	XP_011544097.1:p.Ala1113Pro
XM_011545796.1:c.3337G>C	XP_011544098.1:p.Ala1113Pro
NM_001330520.2:c.3337G>C	NP_001317449.1:p.Ala1113Pro
NM_001351850.1:c.3364G>C	NP_001338779.1:p.Ala1122Pro
NM_014494.3:c.3337G>C	NP_055309.2:p.Ala1113Pro
XM_005255257.4:c.2578G>C	XP_005255314.1:p.Ala860Pro
XM_017023144.2:c.3364G>C	XP_016878633.1:p.Ala1122Pro
XM_017023145.2:c.3364G>C	XP_016878634.1:p.Ala1122Pro
XM_017023146.1:c.3289G>C	XP_016878635.1:p.Ala1097Pro
XM_017023148.2:c.3203-910G>C	XP_016878637.1:n.3203-910G>C
XM_017023150.2:c.3364G>C	XP_016878639.1:p.Ala1122Pro
XM_017023152.2:c.2938G>C	XP_016878641.1:p.Ala980Pro
XM_017023153.1:c.2578G>C	XP_016878642.1:p.Ala860Pro
XM_017023154.1:c.2578G>C	XP_016878643.1:p.Ala860Pro
XM_024450231.1:c.3364G>C	XP_024305999.1:p.Ala1122Pro
XM_024450232.1:c.3364G>C	XP_024306000.1:p.Ala1122Pro
XM_024450233.1:c.3203-910G>C	XP_024306001.1:n.3203-910G>C
NM_014494.4:c.3337G>C MANE Select	NP_055309.2:p.Ala1113Pro
NM_001330520.3:c.3337G>C	NP_001317449.1:p.Ala1113Pro
NM_001351850.2:c.3364G>C	NP_001338779.1:p.Ala1122Pro