Canonical Allele Identifier: CA1465421037
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754371_67754376delinsTGGTGC , CM000666.2:g.67754371_67754376delinsTGGTGC GRCh38
NC_000004.11:g.68620089_68620094delinsTGGTGC , CM000666.1:g.68620089_68620094delinsTGGTGC GRCh37
NC_000004.10:g.68302684_68302689delinsTGGTGC NCBI36
NG_009293.1:g.6711_6716delinsGCACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-41_-36delinsGCACCA MANE Select ENSP00000226413.5:n.-41_-36delinsGCACCA
NM_000406.2:c.-41_-36delinsGCACCA NP_000397.1:n.-41_-36delinsGCACCA
NM_001012763.1:c.-41_-36delinsGCACCA NP_001012781.1:n.-41_-36delinsGCACCA
NM_000406.3:c.-41_-36delinsGCACCA MANE Select NP_000397.1:n.-41_-36delinsGCACCA
NM_001012763.2:c.-41_-36delinsGCACCA NP_001012781.1:n.-41_-36delinsGCACCA