Canonical Allele Identifier: CA2036872409
Gene: RARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53211474C= , CM000674.2:g.53211474C= GRCh38
NC_000012.11:g.53605258C= , CM000674.1:g.53605258C= GRCh37
NC_000012.10:g.51891525C= NCBI36
NG_029822.1:g.25783G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425354.7:c.*202G= MANE Select ENSP00000388510.2:n.*202G=
ENST00000338561.9:c.*202G= ENSP00000343698.5:n.*202G=
ENST00000394426.5:c.*202G= ENSP00000377947.2:n.*202G=
ENST00000425354.6:c.*202G= ENSP00000388510.2:n.*202G=
ENST00000543726.1:c.*202G= ENSP00000444335.1:n.*202G=
ENST00000543762.5:n.1560G=
NM_000966.5:c.*202G= NP_000957.1:n.*202G=
NM_001042728.2:c.*202G= NP_001036193.1:n.*202G=
NM_001243730.1:c.*202G= NP_001230659.1:n.*202G=
NM_001243731.1:c.*202G= NP_001230660.1:n.*202G=
NM_001243732.1:c.*202G= NP_001230661.1:n.*202G=
XM_005269054.2:c.*202G= XP_005269111.1:n.*202G=
XM_005269055.2:c.*202G= XP_005269112.1:n.*202G=
XM_005269056.2:c.*202G= XP_005269113.1:n.*202G=
XM_005269057.1:c.*202G= XP_005269114.1:n.*202G=
XM_011538628.1:c.*202G= XP_011536930.1:n.*202G=
XM_024449112.1:c.*202G= XP_024304880.1:n.*202G=
XM_024449113.1:c.*202G= XP_024304881.1:n.*202G=
XM_024449114.1:c.*202G= XP_024304882.1:n.*202G=
NM_000966.6:c.*202G= MANE Select NP_000957.1:n.*202G=
NM_001042728.3:c.*202G= NP_001036193.1:n.*202G=
NM_001243731.2:c.*202G= NP_001230660.1:n.*202G=
NM_001243732.2:c.*202G= NP_001230661.1:n.*202G=
NM_001243730.2:c.*202G= NP_001230659.1:n.*202G=