Canonical Allele Identifier: CA2762037081
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740530dup , CM000666.2:g.67740530dup GRCh38
NC_000004.11:g.68606248dup , CM000666.1:g.68606248dup GRCh37
NC_000004.10:g.68288843dup NCBI36
NG_009293.1:g.20561dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.941dup MANE Select ENSP00000226413.5:p.Leu314PhefsTer6
ENST00000226413.4:c.941dup ENSP00000226413.4:p.Leu314PhefsTer6
ENST00000420975.2:c.813dup ENSP00000397561.2:n.813dup
NM_000406.2:c.941dup NP_000397.1:p.Leu314PhefsTer6
NM_001012763.1:c.*63dup NP_001012781.1:n.*63dup
NM_000406.3:c.941dup MANE Select NP_000397.1:p.Leu314PhefsTer6
NM_001012763.2:c.*63dup NP_001012781.1:n.*63dup
Search 100 bp 5'
Search 100 bp 3'