Canonical Allele Identifier: CA2530270499
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754183_67754184insCT , CM000666.2:g.67754183_67754184insCT GRCh38
NC_000004.11:g.68619901_68619902insCT , CM000666.1:g.68619901_68619902insCT GRCh37
NC_000004.10:g.68302496_68302497insCT NCBI36
NG_009293.1:g.6903_6904insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.152_153insAG MANE Select ENSP00000226413.5:p.Phe52AlafsTer8
ENST00000226413.4:c.152_153insAG ENSP00000226413.4:p.Phe52AlafsTer8
ENST00000420975.2:c.152_153insAG ENSP00000397561.2:p.Phe52AlafsTer8
NM_000406.2:c.152_153insAG NP_000397.1:p.Phe52AlafsTer8
NM_001012763.1:c.152_153insAG NP_001012781.1:p.Phe52AlafsTer8
NM_000406.3:c.152_153insAG MANE Select NP_000397.1:p.Phe52AlafsTer8
NM_001012763.2:c.152_153insAG NP_001012781.1:p.Phe52AlafsTer8
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