Canonical Allele Identifier: CA2465564797
Gene: GPR50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181313G= , CM000685.2:g.151181313G= GRCh38
NC_000023.10:g.150349785G= , CM000685.1:g.150349785G= GRCh37
NC_000023.9:g.150100443G= NCBI36
NG_016405.1:g.9730G=
NG_016405.2:g.9730G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1730G= MANE Select ENSP00000218316.3:p.Ser577=
ENST00000218316.3:c.1730G= ENSP00000218316.3:p.Ser577=
ENST00000617907.1:c.1724G= ENSP00000484496.1:p.Ser575=
NM_004224.3:c.1730G= MANE Select NP_004215.2:p.Ser577=
XM_011531216.1:c.989G= XP_011529518.1:p.Ser330=
XM_011531216.2:c.989G= XP_011529518.1:p.Ser330=