Canonical Allele Identifier: CA1465420953
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754165_67754169delinsCAAGA , CM000666.2:g.67754165_67754169delinsCAAGA GRCh38
NC_000004.11:g.68619883_68619887delinsCAAGA , CM000666.1:g.68619883_68619887delinsCAAGA GRCh37
NC_000004.10:g.68302478_68302482delinsCAAGA NCBI36
NG_009293.1:g.6918_6922delinsTCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.167_171delinsTCTTG MANE Select ENSP00000226413.5:p.Phe56=
ENST00000226413.4:c.167_171delinsTCTTG ENSP00000226413.4:p.Phe56=
ENST00000420975.2:c.167_171delinsTCTTG ENSP00000397561.2:p.Phe56=
NM_000406.2:c.167_171delinsTCTTG NP_000397.1:p.Phe56=
NM_001012763.1:c.167_171delinsTCTTG NP_001012781.1:p.Phe56=
NM_000406.3:c.167_171delinsTCTTG MANE Select NP_000397.1:p.Phe56=
NM_001012763.2:c.167_171delinsTCTTG NP_001012781.1:p.Phe56=
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