Canonical Allele Identifier: CA7938189

Gene: GPRC5B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.19872808T>C , CM000678.2:g.19872808T>C	GRCh38
NC_000016.9:g.19884130T>C , CM000678.1:g.19884130T>C	GRCh37
NC_000016.8:g.19791631T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016235.3:c.38A>G MANE Select	NP_057319.1:p.Gln13Arg
ENST00000300571.7:c.38A>G MANE Select	ENSP00000300571.2:p.Gln13Arg
NM_001304771.1:c.431A>G	NP_001291700.1:p.Gln144Arg
NM_016235.2:c.38A>G	NP_057319.1:p.Gln13Arg
ENST00000300571.6:c.38A>G	ENSP00000300571.2:p.Gln13Arg
ENST00000535671.5:c.38A>G	ENSP00000442858.1:p.Gln13Arg
ENST00000562469.5:c.38A>G	ENSP00000455960.1:p.Gln13Arg
ENST00000564449.1:c.38A>G	ENSP00000457018.1:p.Gln13Arg
ENST00000566822.1:c.38A>G	ENSP00000454667.1:p.Gln13Arg
ENST00000568214.1:c.38A>G	ENSP00000457080.1:p.Gln13Arg
ENST00000569479.5:c.38A>G	ENSP00000454727.1:p.Gln13Arg
ENST00000569847.1:c.38A>G	ENSP00000457283.1:p.Gln13Arg
ENST00000570142.5:c.38A>G	ENSP00000456724.1:p.Gln13Arg
XM_006721051.2:c.38A>G	XP_006721114.1:p.Gln13Arg
XM_006721051.3:c.38A>G	XP_006721114.1:p.Gln13Arg
XM_006721052.2:c.38A>G	XP_006721115.1:p.Gln13Arg