Canonical Allele Identifier: CA1465408695
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740132_67740133delinsGT , CM000666.2:g.67740132_67740133delinsGT GRCh38
NC_000004.11:g.68605850_68605851delinsGT , CM000666.1:g.68605850_68605851delinsGT GRCh37
NC_000004.10:g.68288445_68288446delinsGT NCBI36
NG_009293.1:g.20954_20955delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*347_*348delinsAC MANE Select ENSP00000226413.5:n.*347_*348delinsAC
ENST00000226413.4:c.*347_*348delinsAC ENSP00000226413.4:n.*347_*348delinsAC
NM_000406.2:c.*347_*348delinsAC NP_000397.1:n.*347_*348delinsAC
NM_001012763.1:c.*456_*457delinsAC NP_001012781.1:n.*456_*457delinsAC
NM_000406.3:c.*347_*348delinsAC MANE Select NP_000397.1:n.*347_*348delinsAC
NM_001012763.2:c.*456_*457delinsAC NP_001012781.1:n.*456_*457delinsAC
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