Canonical Allele Identifier: CA415269976
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349781G>C (hg19) chrX:g.151181309G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181309G>C , CM000685.2:g.151181309G>C GRCh38
NC_000023.10:g.150349781G>C , CM000685.1:g.150349781G>C GRCh37
NC_000023.9:g.150100439G>C NCBI36
NG_016405.1:g.9726G>C
NG_016405.2:g.9726G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1726G>C MANE Select ENSP00000218316.3:p.Ala576Pro
ENST00000218316.3:c.1726G>C ENSP00000218316.3:p.Ala576Pro
ENST00000617907.1:c.1720G>C ENSP00000484496.1:p.Ala574Pro
NM_004224.3:c.1726G>C MANE Select NP_004215.2:p.Ala576Pro
XM_011531216.1:c.985G>C XP_011529518.1:p.Ala329Pro
XM_011531216.2:c.985G>C XP_011529518.1:p.Ala329Pro
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