Canonical Allele Identifier: CA390607448

Gene: GPR68

Linked Data

• MyVariant Identifiers: chr14:g.91701309A>T (hg19) ; chr14:g.91234965A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234965A>T , CM000676.2:g.91234965A>T	GRCh38
NC_000014.8:g.91701309A>T , CM000676.1:g.91701309A>T	GRCh37
NC_000014.7:g.90771062A>T	NCBI36
NG_052988.1:g.23916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.86T>A MANE Select	ENSP00000498702.1:p.Val29Asp
ENST00000529102.1:c.86T>A	ENSP00000432740.1:p.Val29Asp
ENST00000531499.2:c.86T>A	ENSP00000434045.2:p.Val29Asp
ENST00000535815.5:c.86T>A	ENSP00000440797.1:p.Val29Asp
NM_001177676.1:c.86T>A	NP_001171147.1:p.Val29Asp
NM_003485.3:c.86T>A	NP_003476.3:p.Val29Asp
XM_005268110.3:c.116T>A	XP_005268167.1:p.Val39Asp
XM_005268111.2:c.116T>A	XP_005268168.1:p.Val39Asp
XM_005268112.2:c.116T>A	XP_005268169.1:p.Val39Asp
XM_006720262.2:c.116T>A	XP_006720325.1:p.Val39Asp
XM_011537196.1:c.116T>A	XP_011535498.1:p.Val39Asp
XM_011537197.1:c.116T>A	XP_011535499.1:p.Val39Asp
XM_011537198.1:c.116T>A	XP_011535500.1:p.Val39Asp
XM_011537199.1:c.116T>A	XP_011535501.1:p.Val39Asp
XM_011537200.1:c.116T>A	XP_011535502.1:p.Val39Asp
NM_001348437.1:c.86T>A	NP_001335366.1:p.Val29Asp
XM_005268110.4:c.116T>A	XP_005268167.1:p.Val39Asp
XM_005268111.3:c.116T>A	XP_005268168.1:p.Val39Asp
XM_005268112.3:c.116T>A	XP_005268169.1:p.Val39Asp
XM_006720262.3:c.116T>A	XP_006720325.1:p.Val39Asp
XM_011537196.2:c.116T>A	XP_011535498.1:p.Val39Asp
XM_011537197.3:c.116T>A	XP_011535499.1:p.Val39Asp
XM_011537198.2:c.116T>A	XP_011535500.1:p.Val39Asp
XM_011537199.2:c.116T>A	XP_011535501.1:p.Val39Asp
NM_001177676.2:c.86T>A MANE Select	NP_001171147.1:p.Val29Asp