Canonical Allele Identifier: CA1465420933
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754120_67754121delinsCT , CM000666.2:g.67754120_67754121delinsCT GRCh38
NC_000004.11:g.68619838_68619839delinsCT , CM000666.1:g.68619838_68619839delinsCT GRCh37
NC_000004.10:g.68302433_68302434delinsCT NCBI36
NG_009293.1:g.6966_6967delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.215_216delinsAG MANE Select ENSP00000226413.5:p.Lys72=
ENST00000226413.4:c.215_216delinsAG ENSP00000226413.4:p.Lys72=
ENST00000420975.2:c.215_216delinsAG ENSP00000397561.2:p.Lys72=
NM_000406.2:c.215_216delinsAG NP_000397.1:p.Lys72=
NM_001012763.1:c.215_216delinsAG NP_001012781.1:p.Lys72=
NM_000406.3:c.215_216delinsAG MANE Select NP_000397.1:p.Lys72=
NM_001012763.2:c.215_216delinsAG NP_001012781.1:p.Lys72=
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