Canonical Allele Identifier: CA965924128
Gene: GPR68 HGNC NCBI

Linked Data

dbSNP Id: rs1888412634

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91234571_91234573del , CM000676.2:g.91234571_91234573del GRCh38
NC_000014.8:g.91700915_91700917del , CM000676.1:g.91700915_91700917del GRCh37
NC_000014.7:g.90770668_90770670del NCBI36
NG_052988.1:g.24312_24314del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650645.1:c.482_484del MANE Select ENSP00000498702.1:p.Glu161del
ENST00000529102.1:c.482_484del ENSP00000432740.1:p.Glu161del
ENST00000531499.2:c.482_484del ENSP00000434045.2:p.Glu161del
ENST00000535815.5:c.482_484del ENSP00000440797.1:p.Glu161del
NM_001177676.1:c.482_484del NP_001171147.1:p.Glu161del
NM_003485.3:c.482_484del NP_003476.3:p.Glu161del
XM_005268110.3:c.512_514del XP_005268167.1:p.Glu171del
XM_005268111.2:c.512_514del XP_005268168.1:p.Glu171del
XM_005268112.2:c.512_514del XP_005268169.1:p.Glu171del
XM_006720262.2:c.512_514del XP_006720325.1:p.Glu171del
XM_011537196.1:c.512_514del XP_011535498.1:p.Glu171del
XM_011537197.1:c.512_514del XP_011535499.1:p.Glu171del
XM_011537198.1:c.512_514del XP_011535500.1:p.Glu171del
XM_011537199.1:c.512_514del XP_011535501.1:p.Glu171del
XM_011537200.1:c.512_514del XP_011535502.1:p.Glu171del
NM_001348437.1:c.482_484del NP_001335366.1:p.Glu161del
XM_005268110.4:c.512_514del XP_005268167.1:p.Glu171del
XM_005268111.3:c.512_514del XP_005268168.1:p.Glu171del
XM_005268112.3:c.512_514del XP_005268169.1:p.Glu171del
XM_006720262.3:c.512_514del XP_006720325.1:p.Glu171del
XM_011537196.2:c.512_514del XP_011535498.1:p.Glu171del
XM_011537197.3:c.512_514del XP_011535499.1:p.Glu171del
XM_011537198.2:c.512_514del XP_011535500.1:p.Glu171del
XM_011537199.2:c.512_514del XP_011535501.1:p.Glu171del
NM_001177676.2:c.482_484del MANE Select NP_001171147.1:p.Glu161del