Canonical Allele Identifier: CA390606310
Gene: GPR68 HGNC NCBI

Linked Data

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