Canonical Allele Identifier: CA2619016483

Gene: RARG

Linked Data

• gnomAD v4: 12-53211428-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53211428G>A , CM000674.2:g.53211428G>A	GRCh38
NC_000012.11:g.53605212G>A , CM000674.1:g.53605212G>A	GRCh37
NC_000012.10:g.51891479G>A	NCBI36
NG_029822.1:g.25829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425354.7:c.*248C>T MANE Select	ENSP00000388510.2:n.*248C>T
ENST00000338561.9:c.*248C>T	ENSP00000343698.5:n.*248C>T
ENST00000394426.5:c.*248C>T	ENSP00000377947.2:n.*248C>T
ENST00000425354.6:c.*248C>T	ENSP00000388510.2:n.*248C>T
ENST00000543726.1:c.*248C>T	ENSP00000444335.1:n.*248C>T
ENST00000543762.5:n.1606C>T
NM_000966.5:c.*248C>T	NP_000957.1:n.*248C>T
NM_001042728.2:c.*248C>T	NP_001036193.1:n.*248C>T
NM_001243730.1:c.*248C>T	NP_001230659.1:n.*248C>T
NM_001243731.1:c.*248C>T	NP_001230660.1:n.*248C>T
NM_001243732.1:c.*248C>T	NP_001230661.1:n.*248C>T
XM_005269054.2:c.*248C>T	XP_005269111.1:n.*248C>T
XM_005269055.2:c.*248C>T	XP_005269112.1:n.*248C>T
XM_005269056.2:c.*248C>T	XP_005269113.1:n.*248C>T
XM_005269057.1:c.*248C>T	XP_005269114.1:n.*248C>T
XM_011538628.1:c.*248C>T	XP_011536930.1:n.*248C>T
XM_024449112.1:c.*248C>T	XP_024304880.1:n.*248C>T
XM_024449113.1:c.*248C>T	XP_024304881.1:n.*248C>T
XM_024449114.1:c.*248C>T	XP_024304882.1:n.*248C>T
NM_000966.6:c.*248C>T MANE Select	NP_000957.1:n.*248C>T
NM_001042728.3:c.*248C>T	NP_001036193.1:n.*248C>T
NM_001243731.2:c.*248C>T	NP_001230660.1:n.*248C>T
NM_001243732.2:c.*248C>T	NP_001230661.1:n.*248C>T
NM_001243730.2:c.*248C>T	NP_001230659.1:n.*248C>T