Canonical Allele Identifier: CA2154863289

Gene: GPR68

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234747A= , CM000676.2:g.91234747A=	GRCh38
NC_000014.8:g.91701091A= , CM000676.1:g.91701091A=	GRCh37
NC_000014.7:g.90770844A=	NCBI36
NG_052988.1:g.24134T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.304T= MANE Select	ENSP00000498702.1:p.Tyr102=
ENST00000529102.1:c.304T=	ENSP00000432740.1:p.Tyr102=
ENST00000531499.2:c.304T=	ENSP00000434045.2:p.Tyr102=
ENST00000535815.5:c.304T=	ENSP00000440797.1:p.Tyr102=
NM_001177676.1:c.304T=	NP_001171147.1:p.Tyr102=
NM_003485.3:c.304T=	NP_003476.3:p.Tyr102=
XM_005268110.3:c.334T=	XP_005268167.1:p.Tyr112=
XM_005268111.2:c.334T=	XP_005268168.1:p.Tyr112=
XM_005268112.2:c.334T=	XP_005268169.1:p.Tyr112=
XM_006720262.2:c.334T=	XP_006720325.1:p.Tyr112=
XM_011537196.1:c.334T=	XP_011535498.1:p.Tyr112=
XM_011537197.1:c.334T=	XP_011535499.1:p.Tyr112=
XM_011537198.1:c.334T=	XP_011535500.1:p.Tyr112=
XM_011537199.1:c.334T=	XP_011535501.1:p.Tyr112=
XM_011537200.1:c.334T=	XP_011535502.1:p.Tyr112=
NM_001348437.1:c.304T=	NP_001335366.1:p.Tyr102=
XM_005268110.4:c.334T=	XP_005268167.1:p.Tyr112=
XM_005268111.3:c.334T=	XP_005268168.1:p.Tyr112=
XM_005268112.3:c.334T=	XP_005268169.1:p.Tyr112=
XM_006720262.3:c.334T=	XP_006720325.1:p.Tyr112=
XM_011537196.2:c.334T=	XP_011535498.1:p.Tyr112=
XM_011537197.3:c.334T=	XP_011535499.1:p.Tyr112=
XM_011537198.2:c.334T=	XP_011535500.1:p.Tyr112=
XM_011537199.2:c.334T=	XP_011535501.1:p.Tyr112=
NM_001177676.2:c.304T= MANE Select	NP_001171147.1:p.Tyr102=