Canonical Allele Identifier: CA415270023
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349802A>C (hg19) chrX:g.151181330A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181330A>C , CM000685.2:g.151181330A>C GRCh38
NC_000023.10:g.150349802A>C , CM000685.1:g.150349802A>C GRCh37
NC_000023.9:g.150100460A>C NCBI36
NG_016405.1:g.9747A>C
NG_016405.2:g.9747A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218316.4:c.1747A>C MANE Select ENSP00000218316.3:p.Thr583Pro
ENST00000218316.3:c.1747A>C ENSP00000218316.3:p.Thr583Pro
ENST00000617907.1:c.1741A>C ENSP00000484496.1:p.Thr581Pro
NM_004224.3:c.1747A>C MANE Select NP_004215.2:p.Thr583Pro
XM_011531216.1:c.1006A>C XP_011529518.1:p.Thr336Pro
XM_011531216.2:c.1006A>C XP_011529518.1:p.Thr336Pro
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