Canonical Allele Identifier: CA1465421030

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754361_67754362delinsCT , CM000666.2:g.67754361_67754362delinsCT	GRCh38
NC_000004.11:g.68620079_68620080delinsCT , CM000666.1:g.68620079_68620080delinsCT	GRCh37
NC_000004.10:g.68302674_68302675delinsCT	NCBI36
NG_009293.1:g.6725_6726delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-27_-26delinsAG MANE Select	ENSP00000226413.5:n.-27_-26delinsAG
NM_000406.2:c.-27_-26delinsAG	NP_000397.1:n.-27_-26delinsAG
NM_001012763.1:c.-27_-26delinsAG	NP_001012781.1:n.-27_-26delinsAG
NM_000406.3:c.-27_-26delinsAG MANE Select	NP_000397.1:n.-27_-26delinsAG
NM_001012763.2:c.-27_-26delinsAG	NP_001012781.1:n.-27_-26delinsAG