Canonical Allele Identifier: CA1465420934
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731924243

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754125del , CM000666.2:g.67754125del GRCh38
NC_000004.11:g.68619843del , CM000666.1:g.68619843del GRCh37
NC_000004.10:g.68302438del NCBI36
NG_009293.1:g.6966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.215del MANE Select ENSP00000226413.5:p.Lys72SerfsTer5
ENST00000226413.4:c.215del ENSP00000226413.4:p.Lys72SerfsTer5
ENST00000420975.2:c.215del ENSP00000397561.2:p.Lys72SerfsTer5
NM_000406.2:c.215del NP_000397.1:p.Lys72SerfsTer5
NM_001012763.1:c.215del NP_001012781.1:p.Lys72SerfsTer5
NM_000406.3:c.215del MANE Select NP_000397.1:p.Lys72SerfsTer5
NM_001012763.2:c.215del NP_001012781.1:p.Lys72SerfsTer5