Canonical Allele Identifier: CA1620270822

Gene: GRM4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34022602A= , CM000668.2:g.34022602A=	GRCh38
NC_000006.11:g.33990379A= , CM000668.1:g.33990379A=	GRCh37
NC_000006.10:g.34098357A=	NCBI36
NG_029677.3:g.138021T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000538487.7:c.*219T= MANE Select	ENSP00000440556.1:n.*219T=
ENST00000374177.7:c.*219T=	ENSP00000363292.3:n.*219T=
ENST00000374181.8:c.*219T=	ENSP00000363296.4:n.*219T=
ENST00000455714.6:c.*219T=	ENSP00000398456.2:n.*219T=
ENST00000535756.5:c.*219T=	ENSP00000437925.1:n.*219T=
ENST00000538487.6:c.*219T=	ENSP00000440556.1:n.*219T=
ENST00000544773.6:c.*219T=	ENSP00000437730.1:n.*219T=
ENST00000545715.5:n.3007T=
ENST00000609222.5:c.*219T=	ENSP00000477466.1:n.*219T=
ENST00000609860.5:n.3433T=
NM_000841.3:c.*219T=	NP_000832.1:n.*219T=
NM_001256809.2:c.*219T=	NP_001243738.1:n.*219T=
NM_001256811.2:c.*219T=	NP_001243740.1:n.*219T=
NM_001256812.2:c.*219T=	NP_001243741.1:n.*219T=
NM_001256813.2:c.*219T=	NP_001243742.1:n.*219T=
NM_001282847.1:c.*219T=	NP_001269776.1:n.*219T=
XM_011514531.1:c.*219T=	XP_011512833.1:n.*219T=
XM_017010790.2:c.*219T=	XP_016866279.1:n.*219T=
XM_017010791.2:c.*219T=	XP_016866280.1:n.*219T=
XM_017010792.1:c.*219T=	XP_016866281.1:n.*219T=
XM_017010793.2:c.*219T=	XP_016866282.1:n.*219T=
XR_001743363.1:n.3947T=
XR_001743364.2:n.3563T=
NM_000841.4:c.*219T= MANE Select	NP_000832.1:n.*219T=
NM_001256813.3:c.*219T=	NP_001243742.1:n.*219T=
NM_001282847.2:c.*219T=	NP_001269776.1:n.*219T=
NM_001256809.3:c.*219T=	NP_001243738.1:n.*219T=
NM_001256811.3:c.*219T=	NP_001243740.1:n.*219T=