Canonical Allele Identifier: CA1140552539
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539906_100539908delinsCCC , CM000663.2:g.100539906_100539908delinsCCC GRCh38
NC_000001.10:g.101005462_101005464delinsCCC , CM000663.1:g.101005462_101005464delinsCCC GRCh37
NC_000001.9:g.100778050_100778052delinsCCC NCBI36
NG_053134.1:g.6735_6737delinsCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.940_942delinsCCC MANE Select ENSP00000314223.4:p.Pro314=
ENST00000315033.4:c.940_942delinsCCC ENSP00000314223.4:p.Pro314=
NM_022049.2:c.940_942delinsCCC NP_071332.2:p.Pro314=
NM_022049.3:c.940_942delinsCCC MANE Select NP_071332.2:p.Pro314=
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