Canonical Allele Identifier: CA1620306200

Gene: GRM4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34100631G= , CM000668.2:g.34100631G=	GRCh38
NC_000006.11:g.34068408G= , CM000668.1:g.34068408G=	GRCh37
NC_000006.10:g.34176386G=	NCBI36
NG_029677.3:g.59992C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000841.4:c.520-8532C= MANE Select	NP_000832.1:n.520-8532C=
ENST00000538487.7:c.520-8532C= MANE Select	ENSP00000440556.1:n.520-8532C=
NM_000841.3:c.520-8532C=	NP_000832.1:n.520-8532C=
NM_001256809.2:c.313-8532C=	NP_001243738.1:n.313-8532C=
NM_001256809.3:c.313-8532C=	NP_001243738.1:n.313-8532C=
NM_001256811.2:c.520-8532C=	NP_001243740.1:n.520-8532C=
NM_001256811.3:c.520-8532C=	NP_001243740.1:n.520-8532C=
NM_001256812.2:c.13-8532C=	NP_001243741.1:n.13-8532C=
NM_001256813.2:c.120+2950C=	NP_001243742.1:n.120+2950C=
NM_001256813.3:c.120+2950C=	NP_001243742.1:n.120+2950C=
NM_001282847.1:c.-189+32347C=	NP_001269776.1:n.-189+32347C=
NM_001282847.2:c.-189+32347C=	NP_001269776.1:n.-189+32347C=
ENST00000374177.7:c.313-8532C=	ENSP00000363292.3:n.313-8532C=
ENST00000374181.8:c.520-8532C=	ENSP00000363296.4:n.520-8532C=
ENST00000455714.6:c.99+1391C=	ENSP00000398456.2:n.99+1391C=
ENST00000535756.5:c.120+2950C=	ENSP00000437925.1:n.120+2950C=
ENST00000538487.6:c.520-8532C=	ENSP00000440556.1:n.520-8532C=
ENST00000544773.6:c.13-8532C=	ENSP00000437730.1:n.13-8532C=
ENST00000607916.1:n.489-8532C=
ENST00000609222.5:c.120+2950C=	ENSP00000477466.1:n.120+2950C=
ENST00000609278.1:c.519+32347C=	ENSP00000477016.1:n.519+32347C=
ENST00000609973.1:n.45-8532C=
XM_017010790.2:c.520-8532C=	XP_016866279.1:n.520-8532C=
XM_017010791.2:c.520-8532C=	XP_016866280.1:n.520-8532C=
XM_017010792.1:c.279+1391C=	XP_016866281.1:n.279+1391C=
XM_017010793.2:c.120+2950C=	XP_016866282.1:n.120+2950C=
XR_001743363.1:n.1014-8532C=
XR_001743364.2:n.629+2950C=