Canonical Allele Identifier: CA1465408964

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740424A= , CM000666.2:g.67740424A=	GRCh38
NC_000004.11:g.68606142A= , CM000666.1:g.68606142A=	GRCh37
NC_000004.10:g.68288737A=	NCBI36
NG_009293.1:g.20663T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*56T= MANE Select	ENSP00000226413.5:n.*56T=
ENST00000226413.4:c.*56T=	ENSP00000226413.4:n.*56T=
NM_000406.2:c.*56T=	NP_000397.1:n.*56T=
NM_001012763.1:c.*165T=	NP_001012781.1:n.*165T=
NM_000406.3:c.*56T= MANE Select	NP_000397.1:n.*56T=
NM_001012763.2:c.*165T=	NP_001012781.1:n.*165T=