Canonical Allele Identifier: CA1465420939
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754137_67754149delinsTCTTCTGTGTCCA , CM000666.2:g.67754137_67754149delinsTCTTCTGTGTCCA GRCh38
NC_000004.11:g.68619855_68619867delinsTCTTCTGTGTCCA , CM000666.1:g.68619855_68619867delinsTCTTCTGTGTCCA GRCh37
NC_000004.10:g.68302450_68302462delinsTCTTCTGTGTCCA NCBI36
NG_009293.1:g.6938_6950delinsTGGACACAGAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.187_199delinsTGGACACAGAAGA MANE Select ENSP00000226413.5:p.Trp63=
ENST00000226413.4:c.187_199delinsTGGACACAGAAGA ENSP00000226413.4:p.Trp63=
ENST00000420975.2:c.187_199delinsTGGACACAGAAGA ENSP00000397561.2:p.Trp63=
NM_000406.2:c.187_199delinsTGGACACAGAAGA NP_000397.1:p.Trp63=
NM_001012763.1:c.187_199delinsTGGACACAGAAGA NP_001012781.1:p.Trp63=
NM_000406.3:c.187_199delinsTGGACACAGAAGA MANE Select NP_000397.1:p.Trp63=
NM_001012763.2:c.187_199delinsTGGACACAGAAGA NP_001012781.1:p.Trp63=
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