Canonical Allele Identifier: CA1465409188

Gene: GNRHR

Linked Data

• dbSNP Id: rs1731642285

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740671del , CM000666.2:g.67740671del	GRCh38
NC_000004.11:g.68606389del , CM000666.1:g.68606389del	GRCh37
NC_000004.10:g.68288984del	NCBI36
NG_009293.1:g.20416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.796del MANE Select	ENSP00000226413.5:p.Leu266Ter
ENST00000226413.4:c.796del	ENSP00000226413.4:p.Leu266Ter
ENST00000420975.2:c.668del	ENSP00000397561.2:p.Ser223LeufsTer?
NM_000406.2:c.796del	NP_000397.1:p.Leu266Ter
NM_001012763.1:c.668del	NP_001012781.1:p.Ser223LeufsTer?
NM_000406.3:c.796del MANE Select	NP_000397.1:p.Leu266Ter
NM_001012763.2:c.668del	NP_001012781.1:p.Ser223LeufsTer?