Canonical Allele Identifier: CA1529744673
Gene: RETREG1 HGNC NCBI
RETREG1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.16616859T= , CM000667.2:g.16616859T= GRCh38
NC_000005.9:g.16616968T= , CM000667.1:g.16616968T= GRCh37
NC_000005.8:g.16669968T= NCBI36
NG_016644.2:g.5151A= , LRG_363:g.5151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509048.2:n.143A= (RETREG1)
ENST00000682229.1:c.113A= (RETREG1) ENSP00000507342.1:p.Gln38=
ENST00000682564.1:c.113A= (RETREG1) ENSP00000508099.1:p.Gln38=
ENST00000682808.1:n.180A= (RETREG1)
ENST00000682828.1:n.110A= (RETREG1)
ENST00000682982.1:n.136A= (RETREG1)
ENST00000683045.1:n.139A= (RETREG1)
ENST00000683527.1:c.113A= (RETREG1) ENSP00000507253.1:p.Gln38=
ENST00000683973.1:n.139A= (RETREG1)
ENST00000684521.1:c.113A= (RETREG1) ENSP00000507521.1:p.Gln38=
ENST00000684695.1:n.131A= (RETREG1)
ENST00000306320.10:c.113A= (RETREG1) MANE Select ENSP00000304642.9:p.Gln38=
ENST00000306320.9:c.113A= (RETREG1) ENSP00000304642.9:p.Gln38=
ENST00000509048.1:n.180A= (RETREG1)
NM_001034850.2:c.113A= , LRG_363t1:c.113A= (RETREG1) NP_001030022.1:p.Gln38=
NR_109946.1:n.561+373T= (RETREG1-AS1)
XM_011514053.1:c.113A= (RETREG1) XP_011512355.1:p.Gln38=
XM_011514053.3:c.113A= (RETREG1) XP_011512355.1:p.Gln38=
NM_001034850.3:c.113A= (RETREG1) MANE Select NP_001030022.1:p.Gln38=