Canonical Allele Identifier: CA10624075
Gene: RETREG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 352682
ClinVar RCV Id: RCV000351896
dbSNP Id: rs886060393

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.16474618A>C , CM000667.2:g.16474618A>C GRCh38
NC_000005.9:g.16474727A>C , CM000667.1:g.16474727A>C GRCh37
NC_000005.8:g.16527727A>C NCBI36
NG_016644.2:g.147392T>G , LRG_363:g.147392T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509977.2:n.1265T>G
ENST00000510362.6:c.*92+31T>G ENSP00000425089.2:n.*92+31T>G
ENST00000682142.1:c.*123T>G ENSP00000506804.1:n.*123T>G
ENST00000682229.1:c.*123T>G ENSP00000507342.1:n.*123T>G
ENST00000682564.1:c.*123T>G ENSP00000508099.1:n.*123T>G
ENST00000682628.1:c.*123T>G ENSP00000507536.1:n.*123T>G
ENST00000682982.1:n.2391T>G
ENST00000683045.1:n.6161T>G
ENST00000683130.1:c.*863T>G ENSP00000507709.1:n.*863T>G
ENST00000683169.1:n.2116T>G
ENST00000683414.1:c.*123T>G ENSP00000508335.1:n.*123T>G
ENST00000683527.1:c.*916T>G ENSP00000507253.1:n.*916T>G
ENST00000684456.1:c.*123T>G ENSP00000508060.1:n.*123T>G
ENST00000684521.1:c.*123T>G ENSP00000507521.1:n.*123T>G
ENST00000684695.1:n.3887T>G
ENST00000306320.10:c.*123T>G MANE Select ENSP00000304642.9:n.*123T>G
ENST00000306320.9:c.*123T>G ENSP00000304642.9:n.*123T>G
ENST00000399793.6:c.*123T>G ENSP00000382691.2:n.*123T>G
ENST00000510362.5:c.745+31T>G
NM_001034850.2:c.*123T>G , LRG_363t1:c.*123T>G NP_001030022.1:n.*123T>G
NM_019000.4:c.*123T>G NP_061873.2:n.*123T>G
XM_011514053.1:c.*123T>G XP_011512355.1:n.*123T>G
XM_011514054.1:c.*123T>G XP_011512356.1:n.*123T>G
XM_011514055.1:c.*123T>G XP_011512357.1:n.*123T>G
XM_011514053.3:c.*123T>G XP_011512355.1:n.*123T>G
XM_011514054.2:c.*123T>G XP_011512356.1:n.*123T>G
XM_011514055.3:c.*123T>G XP_011512357.1:n.*123T>G
XM_024446117.1:c.*123T>G XP_024301885.1:n.*123T>G
XM_024446118.1:c.*123T>G XP_024301886.1:n.*123T>G
NM_001034850.3:c.*123T>G MANE Select NP_001030022.1:n.*123T>G
NM_019000.5:c.*123T>G NP_061873.2:n.*123T>G