Canonical Allele Identifier: CA1465420364
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753758_67753762delinsTTAGA , CM000666.2:g.67753758_67753762delinsTTAGA GRCh38
NC_000004.11:g.68619476_68619480delinsTTAGA , CM000666.1:g.68619476_68619480delinsTTAGA GRCh37
NC_000004.10:g.68302071_68302075delinsTTAGA NCBI36
NG_009293.1:g.7325_7329delinsTCTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+52_522+56delinsTCTAA MANE Select ENSP00000226413.5:n.522+52_522+56delinsTC...
ENST00000226413.4:c.522+52_522+56delinsTCTAA ENSP00000226413.4:n.522+52_522+56delinsTC...
ENST00000420975.2:c.522+52_522+56delinsTCTAA ENSP00000397561.2:n.522+52_522+56delinsTC...
NM_000406.2:c.522+52_522+56delinsTCTAA NP_000397.1:n.522+52_522+56delinsTCTAA
NM_001012763.1:c.522+52_522+56delinsTCTAA NP_001012781.1:n.522+52_522+56delinsTCTAA...
NM_000406.3:c.522+52_522+56delinsTCTAA MANE Select NP_000397.1:n.522+52_522+56delinsTCTAA
NM_001012763.2:c.522+52_522+56delinsTCTAA NP_001012781.1:n.522+52_522+56delinsTCTAA...
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