Canonical Allele Identifier: CA519131694
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349810T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181338T>A , CM000685.2:g.151181338T>A GRCh38
NC_000023.10:g.150349810T>A , CM000685.1:g.150349810T>A GRCh37
NC_000023.9:g.150100468T>A NCBI36
NG_016405.1:g.9755T>A
NG_016405.2:g.9755T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218316.4:c.1755T>A MANE Select ENSP00000218316.3:p.Ala585=
ENST00000218316.3:c.1755T>A ENSP00000218316.3:p.Ala585=
ENST00000617907.1:c.1749T>A ENSP00000484496.1:p.Ala583=
NM_004224.3:c.1755T>A MANE Select NP_004215.2:p.Ala585=
XM_011531216.1:c.1014T>A XP_011529518.1:p.Ala338=
XM_011531216.2:c.1014T>A XP_011529518.1:p.Ala338=
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