Canonical Allele Identifier: CA552611465

Gene: GNRHR

Linked Data

• dbSNP Id: rs1197293160
• gnomAD v2: 4-68606453-G-GACTAC
• MyVariant Identifiers: chr4:g.68606453_68606454insACTAC (hg19) ; chr4:g.67740735_67740736insACTAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740736_67740737insCTACA , CM000666.2:g.67740736_67740737insCTACA	GRCh38
NC_000004.11:g.68606454_68606455insCTACA , CM000666.1:g.68606454_68606455insCTACA	GRCh37
NC_000004.10:g.68289049_68289050insCTACA	NCBI36
NG_009293.1:g.20351_20352insGTAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.743-12_743-11insGTAGT MANE Select	ENSP00000226413.5:n.743-12_743-11insGTAGT
ENST00000226413.4:c.743-12_743-11insGTAGT	ENSP00000226413.4:n.743-12_743-11insGTAGT
ENST00000420975.2:c.615-12_615-11insGTAGT	ENSP00000397561.2:n.615-12_615-11insGTAGT
NM_000406.2:c.743-12_743-11insGTAGT	NP_000397.1:n.743-12_743-11insGTAGT
NM_001012763.1:c.615-12_615-11insGTAGT	NP_001012781.1:n.615-12_615-11insGTAGT
NM_000406.3:c.743-12_743-11insGTAGT MANE Select	NP_000397.1:n.743-12_743-11insGTAGT
NM_001012763.2:c.615-12_615-11insGTAGT	NP_001012781.1:n.615-12_615-11insGTAGT