Canonical Allele Identifier: CA1162494189

Gene: AGO1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.35897874G>C , CM000663.2:g.35897874G>C	GRCh38
NC_000001.10:g.36363475G>C , CM000663.1:g.36363475G>C	GRCh37
NC_000001.9:g.36136062G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699841.1:c.1020+2605G>C	ENSP00000514639.1:n.1020+2605G>C
ENST00000699842.1:c.*537+2605G>C	ENSP00000514640.1:n.*537+2605G>C
ENST00000699843.1:c.210-3600G>C	ENSP00000514641.1:n.210-3600G>C
ENST00000699844.1:c.817+2605G>C
ENST00000373204.6:c.1020+2605G>C MANE Select	ENSP00000362300.4:n.1020+2605G>C
ENST00000674304.1:c.1020+2605G>C	ENSP00000501450.1:n.1020+2605G>C
ENST00000674426.1:c.1020+2605G>C	ENSP00000501372.1:n.1020+2605G>C
ENST00000373204.5:c.1020+2605G>C	ENSP00000362300.4:n.1020+2605G>C
ENST00000373206.5:c.795+2605G>C	ENSP00000362302.1:n.795+2605G>C
ENST00000635259.1:c.870+2605G>C
NM_012199.2:c.1020+2605G>C	NP_036331.1:n.1020+2605G>C
XM_011541236.1:c.1020+2605G>C	XP_011539538.1:n.1020+2605G>C
XM_011541237.1:c.795+2605G>C	XP_011539539.1:n.795+2605G>C
XM_011541239.1:c.567+2605G>C	XP_011539541.1:n.567+2605G>C
NM_001317122.1:c.1020+2605G>C	NP_001304051.1:n.1020+2605G>C
NM_001317123.1:c.795+2605G>C	NP_001304052.1:n.795+2605G>C
NM_012199.4:c.1020+2605G>C	NP_036331.1:n.1020+2605G>C
XM_011541236.2:c.1020+2605G>C	XP_011539538.1:n.1020+2605G>C
XM_017001016.1:c.1020+2605G>C	XP_016856505.1:n.1020+2605G>C
XM_017001017.1:c.1020+2605G>C	XP_016856506.1:n.1020+2605G>C
XM_017001018.1:c.567+2605G>C	XP_016856507.1:n.567+2605G>C
XM_017001019.1:c.567+2605G>C	XP_016856508.1:n.567+2605G>C
NM_012199.5:c.1020+2605G>C MANE Select	NP_036331.1:n.1020+2605G>C
NM_001317122.2:c.1020+2605G>C	NP_001304051.1:n.1020+2605G>C
NM_001317123.2:c.795+2605G>C	NP_001304052.1:n.795+2605G>C