Canonical Allele Identifier: CA1529744672
Gene: RETREG1 HGNC NCBI
RETREG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.16616855C= , CM000667.2:g.16616855C= GRCh38
NC_000005.9:g.16616964C= , CM000667.1:g.16616964C= GRCh37
NC_000005.8:g.16669964C= NCBI36
NG_016644.2:g.5155G= , LRG_363:g.5155G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509048.2:n.147G= (RETREG1)
ENST00000682229.1:c.117G= (RETREG1) ENSP00000507342.1:p.Gln39=
ENST00000682564.1:c.117G= (RETREG1) ENSP00000508099.1:p.Gln39=
ENST00000682808.1:n.184G= (RETREG1)
ENST00000682828.1:n.114G= (RETREG1)
ENST00000682982.1:n.140G= (RETREG1)
ENST00000683045.1:n.143G= (RETREG1)
ENST00000683527.1:c.117G= (RETREG1) ENSP00000507253.1:p.Gln39=
ENST00000683973.1:n.143G= (RETREG1)
ENST00000684521.1:c.117G= (RETREG1) ENSP00000507521.1:p.Gln39=
ENST00000684695.1:n.135G= (RETREG1)
ENST00000306320.10:c.117G= (RETREG1) MANE Select ENSP00000304642.9:p.Gln39=
ENST00000306320.9:c.117G= (RETREG1) ENSP00000304642.9:p.Gln39=
ENST00000509048.1:n.184G= (RETREG1)
NM_001034850.2:c.117G= , LRG_363t1:c.117G= (RETREG1) NP_001030022.1:p.Gln39=
NR_109946.1:n.561+369C= (RETREG1-AS1)
XM_011514053.1:c.117G= (RETREG1) XP_011512355.1:p.Gln39=
XM_011514053.3:c.117G= (RETREG1) XP_011512355.1:p.Gln39=
NM_001034850.3:c.117G= (RETREG1) MANE Select NP_001030022.1:p.Gln39=