Canonical Allele Identifier: CA1465420366
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731912661
gnomAD v4: 4-67753758-TTAGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753762_67753765del , CM000666.2:g.67753762_67753765del GRCh38
NC_000004.11:g.68619480_68619483del , CM000666.1:g.68619480_68619483del GRCh37
NC_000004.10:g.68302075_68302078del NCBI36
NG_009293.1:g.7325_7328del

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+52_522+55del MANE Select ENSP00000226413.5:n.522+52_522+55del
ENST00000226413.4:c.522+52_522+55del ENSP00000226413.4:n.522+52_522+55del
ENST00000420975.2:c.522+52_522+55del ENSP00000397561.2:n.522+52_522+55del
NM_000406.2:c.522+52_522+55del NP_000397.1:n.522+52_522+55del
NM_001012763.1:c.522+52_522+55del NP_001012781.1:n.522+52_522+55del
NM_000406.3:c.522+52_522+55del MANE Select NP_000397.1:n.522+52_522+55del
NM_001012763.2:c.522+52_522+55del NP_001012781.1:n.522+52_522+55del
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