Canonical Allele Identifier: CA2670819810

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740692-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740696_67740697del , CM000666.2:g.67740696_67740697del	GRCh38
NC_000004.11:g.68606414_68606415del , CM000666.1:g.68606414_68606415del	GRCh37
NC_000004.10:g.68289009_68289010del	NCBI36
NG_009293.1:g.20393_20394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.773_774del MANE Select	ENSP00000226413.5:p.Ile258ThrfsTer?
ENST00000226413.4:c.773_774del	ENSP00000226413.4:p.Ile258ThrfsTer?
ENST00000420975.2:c.645_646del	ENSP00000397561.2:p.Thr216GlnfsTer5
NM_000406.2:c.773_774del	NP_000397.1:p.Ile258ThrfsTer?
NM_001012763.1:c.645_646del	NP_001012781.1:p.Thr216GlnfsTer5
NM_000406.3:c.773_774del MANE Select	NP_000397.1:p.Ile258ThrfsTer?
NM_001012763.2:c.645_646del	NP_001012781.1:p.Thr216GlnfsTer5