Canonical Allele Identifier: CA2619016579

Gene: RARG

Linked Data

• gnomAD v4: 12-53211460-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53211460G>T , CM000674.2:g.53211460G>T	GRCh38
NC_000012.11:g.53605244G>T , CM000674.1:g.53605244G>T	GRCh37
NC_000012.10:g.51891511G>T	NCBI36
NG_029822.1:g.25797C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425354.7:c.*216C>A MANE Select	ENSP00000388510.2:n.*216C>A
ENST00000338561.9:c.*216C>A	ENSP00000343698.5:n.*216C>A
ENST00000394426.5:c.*216C>A	ENSP00000377947.2:n.*216C>A
ENST00000425354.6:c.*216C>A	ENSP00000388510.2:n.*216C>A
ENST00000543726.1:c.*216C>A	ENSP00000444335.1:n.*216C>A
ENST00000543762.5:n.1574C>A
NM_000966.5:c.*216C>A	NP_000957.1:n.*216C>A
NM_001042728.2:c.*216C>A	NP_001036193.1:n.*216C>A
NM_001243730.1:c.*216C>A	NP_001230659.1:n.*216C>A
NM_001243731.1:c.*216C>A	NP_001230660.1:n.*216C>A
NM_001243732.1:c.*216C>A	NP_001230661.1:n.*216C>A
XM_005269054.2:c.*216C>A	XP_005269111.1:n.*216C>A
XM_005269055.2:c.*216C>A	XP_005269112.1:n.*216C>A
XM_005269056.2:c.*216C>A	XP_005269113.1:n.*216C>A
XM_005269057.1:c.*216C>A	XP_005269114.1:n.*216C>A
XM_011538628.1:c.*216C>A	XP_011536930.1:n.*216C>A
XM_024449112.1:c.*216C>A	XP_024304880.1:n.*216C>A
XM_024449113.1:c.*216C>A	XP_024304881.1:n.*216C>A
XM_024449114.1:c.*216C>A	XP_024304882.1:n.*216C>A
NM_000966.6:c.*216C>A MANE Select	NP_000957.1:n.*216C>A
NM_001042728.3:c.*216C>A	NP_001036193.1:n.*216C>A
NM_001243731.2:c.*216C>A	NP_001230660.1:n.*216C>A
NM_001243732.2:c.*216C>A	NP_001230661.1:n.*216C>A
NM_001243730.2:c.*216C>A	NP_001230659.1:n.*216C>A