Canonical Allele Identifier: CA226554991
Gene: GRM5 HGNC NCBI

Linked Data

dbSNP Id: rs5016282
MyVariant Identifiers: chr11:g.88741660A>G (hg19) chr11:g.89008492A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89008492A>G , CM000673.2:g.89008492A>G GRCh38
NC_000011.9:g.88741660A>G , CM000673.1:g.88741660A>G GRCh37
NC_000011.8:g.88381308A>G NCBI36
NG_052831.1:g.62480T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305447.5:c.661+38720T>C MANE Select ENSP00000306138.4:n.661+38720T>C
ENST00000305432.9:c.661+38720T>C ENSP00000305905.5:n.661+38720T>C
ENST00000305447.4:c.661+38720T>C ENSP00000306138.4:n.661+38720T>C
ENST00000393294.3:c.725+543T>C ENSP00000376972.3:n.725+543T>C
ENST00000449371.6:c.223+543T>C
ENST00000455756.6:c.661+38720T>C ENSP00000405690.2:n.661+38720T>C
NM_000842.4:c.661+38720T>C NP_000833.1:n.661+38720T>C
NM_001143831.2:c.661+38720T>C NP_001137303.1:n.661+38720T>C
XM_006718828.2:c.661+38720T>C XP_006718891.1:n.661+38720T>C
XM_011542792.1:c.661+38720T>C XP_011541094.1:n.661+38720T>C
XM_011542793.1:c.661+38720T>C XP_011541095.1:n.661+38720T>C
XM_011542794.1:c.661+38720T>C XP_011541096.1:n.661+38720T>C
XM_011542795.1:c.661+38720T>C XP_011541097.1:n.661+38720T>C
XM_006718828.4:c.661+38720T>C XP_006718891.1:n.661+38720T>C
XM_017017627.2:c.661+38720T>C XP_016873116.1:n.661+38720T>C
NM_000842.5:c.661+38720T>C NP_000833.1:n.661+38720T>C
NM_001143831.3:c.661+38720T>C MANE Select NP_001137303.1:n.661+38720T>C
NM_001384268.1:c.661+38720T>C NP_001371197.1:n.661+38720T>C
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