Canonical Allele Identifier: CA1209973044
Gene: RALGPS2 HGNC NCBI
RALGPS2-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.178727615T>A , CM000663.2:g.178727615T>A GRCh38
NC_000001.10:g.178696750T>A , CM000663.1:g.178696750T>A GRCh37
NC_000001.9:g.176963373T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367634.7:c.-84+2196T>A (RALGPS2) ENSP00000356606.2:n.-84+2196T>A
ENST00000367635.8:c.-84+2196T>A (RALGPS2) MANE Select ENSP00000356607.3:n.-84+2196T>A
ENST00000324778.5:c.-84+2196T>A (RALGPS2) ENSP00000313613.5:n.-84+2196T>A
ENST00000367634.6:c.-84+2196T>A (RALGPS2) ENSP00000356606.2:n.-84+2196T>A
ENST00000367635.7:c.-84+2196T>A (RALGPS2) ENSP00000356607.3:n.-84+2196T>A
ENST00000495034.5:n.255+2196T>A (RALGPS2)
NM_001286247.1:c.-84+2196T>A (RALGPS2) NP_001273176.1:n.-84+2196T>A
NM_152663.4:c.-84+2196T>A (RALGPS2) NP_689876.2:n.-84+2196T>A
XM_006711410.2:c.-84+1410T>A (RALGPS2) XP_006711473.1:n.-84+1410T>A
XM_011509688.1:c.-84+2196T>A (RALGPS2) XP_011507990.1:n.-84+2196T>A
XM_006711410.3:c.-84+1410T>A (RALGPS2) XP_006711473.1:n.-84+1410T>A
XM_017001591.2:c.-557+2196T>A (RALGPS2) XP_016857080.1:n.-557+2196T>A
XR_002958385.1:n.2317A>T (RALGPS2-AS1)
NM_152663.5:c.-84+2196T>A (RALGPS2) MANE Select NP_689876.2:n.-84+2196T>A
NM_001286247.2:c.-84+2196T>A (RALGPS2) NP_001273176.1:n.-84+2196T>A
NM_001400042.1:c.-84+2196T>A (RALGPS2) NP_001386971.1:n.-84+2196T>A
NR_174383.1:n.176+2196T>A (RALGPS2)
NR_174384.1:n.176+2196T>A (RALGPS2)
Search 100 bp 5'
Search 100 bp 3'