Canonical Allele Identifier: CA346847608

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53854630C>T , CM000664.2:g.53854630C>T GRCh38
NC_000002.11:g.54081767C>T , CM000664.1:g.54081767C>T GRCh37
NC_000002.10:g.53935271C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394705.3:c.127G>A (GPR75) MANE Select ENSP00000378195.2:p.Val43Met
ENST00000406625.6:c.-14+5198G>A (ASB3) ENSP00000385085.4:n.-14+5198G>A
ENST00000394705.2:c.127G>A (GPR75) ENSP00000378195.2:p.Val43Met
ENST00000406625.5:c.101+5198G>A (GPR75-ASB3) ENSP00000385085.3:n.101+5198G>A
ENST00000459916.1:n.93+5198G>A (GPR75-ASB3)
ENST00000498475.2:n.163+5198G>A (GPR75-ASB3)
NM_001164165.1:c.101+5198G>A (GPR75-ASB3) NP_001157637.1:n.101+5198G>A
NM_006794.3:c.127G>A (GPR75) NP_006785.1:p.Val43Met
NM_006794.4:c.127G>A (GPR75) MANE Select NP_006785.1:p.Val43Met
NM_001164165.2:c.101+5198G>A (GPR75-ASB3) NP_001157637.1:n.101+5198G>A