Canonical Allele Identifier: CA226342002
Gene: GRM5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88588556C>T , CM000673.2:g.88588556C>T GRCh38
NC_000011.9:g.88321724C>T , CM000673.1:g.88321724C>T GRCh37
NC_000011.8:g.87961372C>T NCBI36
NG_052831.1:g.482416G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305447.5:c.1690+2045G>A MANE Select ENSP00000306138.4:n.1690+2045G>A
ENST00000305432.9:c.1690+2045G>A ENSP00000305905.5:n.1690+2045G>A
ENST00000305447.4:c.1690+2045G>A ENSP00000306138.4:n.1690+2045G>A
ENST00000455756.6:c.1690+2045G>A ENSP00000405690.2:n.1690+2045G>A
NM_000842.4:c.1690+2045G>A NP_000833.1:n.1690+2045G>A
NM_001143831.2:c.1690+2045G>A NP_001137303.1:n.1690+2045G>A
XM_006718828.2:c.1690+2045G>A XP_006718891.1:n.1690+2045G>A
XM_011542792.1:c.1690+2045G>A XP_011541094.1:n.1690+2045G>A
XM_011542793.1:c.1690+2045G>A XP_011541095.1:n.1690+2045G>A
XM_011542794.1:c.1690+2045G>A XP_011541096.1:n.1690+2045G>A
XM_011542795.1:c.1690+2045G>A XP_011541097.1:n.1690+2045G>A
XM_006718828.4:c.1690+2045G>A XP_006718891.1:n.1690+2045G>A
XM_017017627.2:c.1690+2045G>A XP_016873116.1:n.1690+2045G>A
NM_000842.5:c.1690+2045G>A NP_000833.1:n.1690+2045G>A
NM_001143831.3:c.1690+2045G>A MANE Select NP_001137303.1:n.1690+2045G>A
NM_001384268.1:c.1690+2045G>A NP_001371197.1:n.1690+2045G>A
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