Canonical Allele Identifier: CA2573150274

Gene: GPR68

Linked Data

• ClinVar Variation Id: 1326287
• ClinVar RCV Id: RCV002250378
• dbSNP Id: rs2140845247

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234968_91234973delinsG , CM000676.2:g.91234968_91234973delinsG	GRCh38
NC_000014.8:g.91701312_91701317delinsG , CM000676.1:g.91701312_91701317delinsG	GRCh37
NC_000014.7:g.90771065_90771070delinsG	NCBI36
NG_052988.1:g.23908_23913delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.78_83delinsC MANE Select	ENSP00000498702.1:p.Val27CysfsTer?
ENST00000529102.1:c.78_83delinsC	ENSP00000432740.1:p.Val27CysfsTer?
ENST00000531499.2:c.78_83delinsC	ENSP00000434045.2:p.Val27CysfsTer?
ENST00000535815.5:c.78_83delinsC	ENSP00000440797.1:p.Val27CysfsTer?
NM_001177676.1:c.78_83delinsC	NP_001171147.1:p.Val27CysfsTer?
NM_003485.3:c.78_83delinsC	NP_003476.3:p.Val27CysfsTer?
XM_005268110.3:c.108_113delinsC	XP_005268167.1:p.Val37CysfsTer?
XM_005268111.2:c.108_113delinsC	XP_005268168.1:p.Val37CysfsTer?
XM_005268112.2:c.108_113delinsC	XP_005268169.1:p.Val37CysfsTer?
XM_006720262.2:c.108_113delinsC	XP_006720325.1:p.Val37CysfsTer?
XM_011537196.1:c.108_113delinsC	XP_011535498.1:p.Val37CysfsTer?
XM_011537197.1:c.108_113delinsC	XP_011535499.1:p.Val37CysfsTer?
XM_011537198.1:c.108_113delinsC	XP_011535500.1:p.Val37CysfsTer?
XM_011537199.1:c.108_113delinsC	XP_011535501.1:p.Val37CysfsTer?
XM_011537200.1:c.108_113delinsC	XP_011535502.1:p.Val37CysfsTer?
NM_001348437.1:c.78_83delinsC	NP_001335366.1:p.Val27CysfsTer?
XM_005268110.4:c.108_113delinsC	XP_005268167.1:p.Val37CysfsTer?
XM_005268111.3:c.108_113delinsC	XP_005268168.1:p.Val37CysfsTer?
XM_005268112.3:c.108_113delinsC	XP_005268169.1:p.Val37CysfsTer?
XM_006720262.3:c.108_113delinsC	XP_006720325.1:p.Val37CysfsTer?
XM_011537196.2:c.108_113delinsC	XP_011535498.1:p.Val37CysfsTer?
XM_011537197.3:c.108_113delinsC	XP_011535499.1:p.Val37CysfsTer?
XM_011537198.2:c.108_113delinsC	XP_011535500.1:p.Val37CysfsTer?
XM_011537199.2:c.108_113delinsC	XP_011535501.1:p.Val37CysfsTer?
NM_001177676.2:c.78_83delinsC MANE Select	NP_001171147.1:p.Val27CysfsTer?