Canonical Allele Identifier: CA2678322657

Gene: GRM4

Linked Data

• gnomAD v4: 6-34022480-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34022480G>A , CM000668.2:g.34022480G>A	GRCh38
NC_000006.11:g.33990257G>A , CM000668.1:g.33990257G>A	GRCh37
NC_000006.10:g.34098235G>A	NCBI36
NG_029677.3:g.138143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538487.7:c.*341C>T MANE Select	ENSP00000440556.1:n.*341C>T
ENST00000374177.7:c.*341C>T	ENSP00000363292.3:n.*341C>T
ENST00000374181.8:c.*341C>T	ENSP00000363296.4:n.*341C>T
ENST00000535756.5:c.*341C>T	ENSP00000437925.1:n.*341C>T
ENST00000538487.6:c.*341C>T	ENSP00000440556.1:n.*341C>T
ENST00000544773.6:c.*341C>T	ENSP00000437730.1:n.*341C>T
ENST00000545715.5:n.3129C>T
ENST00000609222.5:c.*341C>T	ENSP00000477466.1:n.*341C>T
ENST00000609860.5:n.3555C>T
NM_000841.3:c.*341C>T	NP_000832.1:n.*341C>T
NM_001256809.2:c.*341C>T	NP_001243738.1:n.*341C>T
NM_001256811.2:c.*341C>T	NP_001243740.1:n.*341C>T
NM_001256812.2:c.*341C>T	NP_001243741.1:n.*341C>T
NM_001256813.2:c.*341C>T	NP_001243742.1:n.*341C>T
NM_001282847.1:c.*341C>T	NP_001269776.1:n.*341C>T
XM_011514531.1:c.*341C>T	XP_011512833.1:n.*341C>T
XM_017010790.2:c.*341C>T	XP_016866279.1:n.*341C>T
XM_017010791.2:c.*341C>T	XP_016866280.1:n.*341C>T
XM_017010792.1:c.*341C>T	XP_016866281.1:n.*341C>T
XM_017010793.2:c.*341C>T	XP_016866282.1:n.*341C>T
XR_001743363.1:n.4069C>T
XR_001743364.2:n.3685C>T
NM_000841.4:c.*341C>T MANE Select	NP_000832.1:n.*341C>T
NM_001256813.3:c.*341C>T	NP_001243742.1:n.*341C>T
NM_001282847.2:c.*341C>T	NP_001269776.1:n.*341C>T
NM_001256809.3:c.*341C>T	NP_001243738.1:n.*341C>T
NM_001256811.3:c.*341C>T	NP_001243740.1:n.*341C>T