Canonical Allele Identifier: CA1465409181
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731642069
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740670dup , CM000666.2:g.67740670dup GRCh38
NC_000004.11:g.68606388dup , CM000666.1:g.68606388dup GRCh37
NC_000004.10:g.68288983dup NCBI36
NG_009293.1:g.20417dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.797dup MANE Select ENSP00000226413.5:p.Met268AsnfsTer26
ENST00000226413.4:c.797dup ENSP00000226413.4:p.Met268AsnfsTer26
ENST00000420975.2:c.669dup ENSP00000397561.2:p.Lys224Ter
NM_000406.2:c.797dup NP_000397.1:p.Met268AsnfsTer26
NM_001012763.1:c.669dup NP_001012781.1:p.Lys224Ter
NM_000406.3:c.797dup MANE Select NP_000397.1:p.Met268AsnfsTer26
NM_001012763.2:c.669dup NP_001012781.1:p.Lys224Ter
Search 100 bp 5'
Search 100 bp 3'