Canonical Allele Identifier: CA1723254424

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86696014_86696015delinsTC , CM000669.2:g.86696014_86696015delinsTC	GRCh38
NC_000007.13:g.86325330_86325331delinsTC , CM000669.1:g.86325330_86325331delinsTC	GRCh37
NC_000007.12:g.86163266_86163267delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.-141+51142_-141+51143delinsTC MANE Select	ENSP00000355316.2:n.-141+51142_-141+51143delinsTC
ENST00000361669.6:c.-141+51142_-141+51143delinsTC	ENSP00000355316.2:n.-141+51142_-141+51143delinsTC
ENST00000421579.1:c.-141+51043_-141+51044delinsTC	ENSP00000390037.1:n.-141+51043_-141+51044delinsTC
ENST00000439827.1:c.-141+51142_-141+51143delinsTC	ENSP00000398767.1:n.-141+51142_-141+51143delinsTC
ENST00000454217.1:c.84+51142_84+51143delinsTC	ENSP00000405427.1:n.84+51142_84+51143delinsTC
NM_000840.2:c.-141+51142_-141+51143delinsTC	NP_000831.2:n.-141+51142_-141+51143delinsTC
XM_011516088.1:c.-141+51142_-141+51143delinsTC	XP_011514390.1:n.-141+51142_-141+51143delinsTC
XM_011516089.1:c.-141+51142_-141+51143delinsTC	XP_011514391.1:n.-141+51142_-141+51143delinsTC
XM_011516090.1:c.-141+51142_-141+51143delinsTC	XP_011514392.1:n.-141+51142_-141+51143delinsTC
NM_001363522.1:c.-141+51142_-141+51143delinsTC	NP_001350451.1:n.-141+51142_-141+51143delinsTC
XM_017012073.2:c.-141+51142_-141+51143delinsTC	XP_016867562.1:n.-141+51142_-141+51143delinsTC
NM_000840.3:c.-141+51142_-141+51143delinsTC MANE Select	NP_000831.2:n.-141+51142_-141+51143delinsTC
NM_001363522.2:c.-141+51142_-141+51143delinsTC	NP_001350451.1:n.-141+51142_-141+51143delinsTC