Canonical Allele Identifier: CA390606310

Gene: GPR68

Linked Data

• gnomAD v4: 14-91234567-C-A
• MyVariant Identifiers: chr14:g.91700911C>A (hg19) ; chr14:g.91234567C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234567C>A , CM000676.2:g.91234567C>A	GRCh38
NC_000014.8:g.91700911C>A , CM000676.1:g.91700911C>A	GRCh37
NC_000014.7:g.90770664C>A	NCBI36
NG_052988.1:g.24314G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.484G>T MANE Select	ENSP00000498702.1:p.Val162Phe
ENST00000529102.1:c.484G>T	ENSP00000432740.1:p.Val162Phe
ENST00000531499.2:c.484G>T	ENSP00000434045.2:p.Val162Phe
ENST00000535815.5:c.484G>T	ENSP00000440797.1:p.Val162Phe
NM_001177676.1:c.484G>T	NP_001171147.1:p.Val162Phe
NM_003485.3:c.484G>T	NP_003476.3:p.Val162Phe
XM_005268110.3:c.514G>T	XP_005268167.1:p.Val172Phe
XM_005268111.2:c.514G>T	XP_005268168.1:p.Val172Phe
XM_005268112.2:c.514G>T	XP_005268169.1:p.Val172Phe
XM_006720262.2:c.514G>T	XP_006720325.1:p.Val172Phe
XM_011537196.1:c.514G>T	XP_011535498.1:p.Val172Phe
XM_011537197.1:c.514G>T	XP_011535499.1:p.Val172Phe
XM_011537198.1:c.514G>T	XP_011535500.1:p.Val172Phe
XM_011537199.1:c.514G>T	XP_011535501.1:p.Val172Phe
XM_011537200.1:c.514G>T	XP_011535502.1:p.Val172Phe
NM_001348437.1:c.484G>T	NP_001335366.1:p.Val162Phe
XM_005268110.4:c.514G>T	XP_005268167.1:p.Val172Phe
XM_005268111.3:c.514G>T	XP_005268168.1:p.Val172Phe
XM_005268112.3:c.514G>T	XP_005268169.1:p.Val172Phe
XM_006720262.3:c.514G>T	XP_006720325.1:p.Val172Phe
XM_011537196.2:c.514G>T	XP_011535498.1:p.Val172Phe
XM_011537197.3:c.514G>T	XP_011535499.1:p.Val172Phe
XM_011537198.2:c.514G>T	XP_011535500.1:p.Val172Phe
XM_011537199.2:c.514G>T	XP_011535501.1:p.Val172Phe
NM_001177676.2:c.484G>T MANE Select	NP_001171147.1:p.Val162Phe