Canonical Allele Identifier: CA2694945942
Gene: GPR50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181416_151181424del , CM000685.2:g.151181416_151181424del GRCh38
NC_000023.10:g.150349888_150349896del , CM000685.1:g.150349888_150349896del GRCh37
NC_000023.9:g.150100546_150100554del NCBI36
NG_016405.1:g.9833_9841del
NG_016405.2:g.9833_9841del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218316.4:c.1833_1841del MANE Select ENSP00000218316.3:p.Asp611_Asp613del
ENST00000218316.3:c.1833_1841del ENSP00000218316.3:p.Asp611_Asp613del
ENST00000617907.1:c.1827_1835del ENSP00000484496.1:p.Asp609_Asp611del
NM_004224.3:c.1833_1841del MANE Select NP_004215.2:p.Asp611_Asp613del
XM_011531216.1:c.1092_1100del XP_011529518.1:p.Asp364_Asp366del
XM_011531216.2:c.1092_1100del XP_011529518.1:p.Asp364_Asp366del