Canonical Allele Identifier: CA357054533

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67753911-G-T
• MyVariant Identifiers: chr4:g.68619629G>T (hg19) ; chr4:g.67753911G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753911G>T , CM000666.2:g.67753911G>T	GRCh38
NC_000004.11:g.68619629G>T , CM000666.1:g.68619629G>T	GRCh37
NC_000004.10:g.68302224G>T	NCBI36
NG_009293.1:g.7176C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.425C>A MANE Select	ENSP00000226413.5:p.Ala142Asp
ENST00000226413.4:c.425C>A	ENSP00000226413.4:p.Ala142Asp
ENST00000420975.2:c.425C>A	ENSP00000397561.2:p.Ala142Asp
NM_000406.2:c.425C>A	NP_000397.1:p.Ala142Asp
NM_001012763.1:c.425C>A	NP_001012781.1:p.Ala142Asp
NM_000406.3:c.425C>A MANE Select	NP_000397.1:p.Ala142Asp
NM_001012763.2:c.425C>A	NP_001012781.1:p.Ala142Asp