Canonical Allele Identifier: CA136960622

Gene: GRM4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34101146G>A , CM000668.2:g.34101146G>A	GRCh38
NC_000006.11:g.34068923G>A , CM000668.1:g.34068923G>A	GRCh37
NC_000006.10:g.34176901G>A	NCBI36
NG_029677.3:g.59477C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538487.7:c.520-9047C>T MANE Select	ENSP00000440556.1:n.520-9047C>T
ENST00000374177.7:c.313-9047C>T	ENSP00000363292.3:n.313-9047C>T
ENST00000374181.8:c.520-9047C>T	ENSP00000363296.4:n.520-9047C>T
ENST00000455714.6:c.99+876C>T	ENSP00000398456.2:n.99+876C>T
ENST00000535756.5:c.120+2435C>T	ENSP00000437925.1:n.120+2435C>T
ENST00000538487.6:c.520-9047C>T	ENSP00000440556.1:n.520-9047C>T
ENST00000544773.6:c.13-9047C>T	ENSP00000437730.1:n.13-9047C>T
ENST00000607916.1:n.489-9047C>T
ENST00000609222.5:c.120+2435C>T	ENSP00000477466.1:n.120+2435C>T
ENST00000609278.1:c.519+31832C>T	ENSP00000477016.1:n.519+31832C>T
ENST00000609973.1:n.45-9047C>T
NM_000841.3:c.520-9047C>T	NP_000832.1:n.520-9047C>T
NM_001256809.2:c.313-9047C>T	NP_001243738.1:n.313-9047C>T
NM_001256811.2:c.520-9047C>T	NP_001243740.1:n.520-9047C>T
NM_001256812.2:c.13-9047C>T	NP_001243741.1:n.13-9047C>T
NM_001256813.2:c.120+2435C>T	NP_001243742.1:n.120+2435C>T
NM_001282847.1:c.-189+31832C>T	NP_001269776.1:n.-189+31832C>T
XM_017010790.2:c.520-9047C>T	XP_016866279.1:n.520-9047C>T
XM_017010791.2:c.520-9047C>T	XP_016866280.1:n.520-9047C>T
XM_017010792.1:c.279+876C>T	XP_016866281.1:n.279+876C>T
XM_017010793.2:c.120+2435C>T	XP_016866282.1:n.120+2435C>T
XR_001743363.1:n.1014-9047C>T
XR_001743364.2:n.629+2435C>T
NM_000841.4:c.520-9047C>T MANE Select	NP_000832.1:n.520-9047C>T
NM_001256813.3:c.120+2435C>T	NP_001243742.1:n.120+2435C>T
NM_001282847.2:c.-189+31832C>T	NP_001269776.1:n.-189+31832C>T
NM_001256809.3:c.313-9047C>T	NP_001243738.1:n.313-9047C>T
NM_001256811.3:c.520-9047C>T	NP_001243740.1:n.520-9047C>T