Canonical Allele Identifier: CA2559420397

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740734_67740735insTTTTTCTCT , CM000666.2:g.67740734_67740735insTTTTTCTCT	GRCh38
NC_000004.11:g.68606452_68606453insTTTTTCTCT , CM000666.1:g.68606452_68606453insTTTTTCTCT	GRCh37
NC_000004.10:g.68289047_68289048insTTTTTCTCT	NCBI36
NG_009293.1:g.20352_20353insAGAGAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.743-11_743-10insAGAGAAAAA MANE Select	ENSP00000226413.5:n.743-11_743-10insAGAGAAAAA
ENST00000226413.4:c.743-11_743-10insAGAGAAAAA	ENSP00000226413.4:n.743-11_743-10insAGAGAAAAA
ENST00000420975.2:c.615-11_615-10insAGAGAAAAA	ENSP00000397561.2:n.615-11_615-10insAGAGAAAAA
NM_000406.2:c.743-11_743-10insAGAGAAAAA	NP_000397.1:n.743-11_743-10insAGAGAAAAA
NM_001012763.1:c.615-11_615-10insAGAGAAAAA	NP_001012781.1:n.615-11_615-10insAGAGAAAAA
NM_000406.3:c.743-11_743-10insAGAGAAAAA MANE Select	NP_000397.1:n.743-11_743-10insAGAGAAAAA
NM_001012763.2:c.615-11_615-10insAGAGAAAAA	NP_001012781.1:n.615-11_615-10insAGAGAAAAA