Canonical Allele Identifier: CA357054567

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67753923-T-A
• MyVariant Identifiers: chr4:g.68619641T>A (hg19) ; chr4:g.67753923T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753923T>A , CM000666.2:g.67753923T>A	GRCh38
NC_000004.11:g.68619641T>A , CM000666.1:g.68619641T>A	GRCh37
NC_000004.10:g.68302236T>A	NCBI36
NG_009293.1:g.7164A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.413A>T MANE Select	ENSP00000226413.5:p.Asp138Val
ENST00000226413.4:c.413A>T	ENSP00000226413.4:p.Asp138Val
ENST00000420975.2:c.413A>T	ENSP00000397561.2:p.Asp138Val
NM_000406.2:c.413A>T	NP_000397.1:p.Asp138Val
NM_001012763.1:c.413A>T	NP_001012781.1:p.Asp138Val
NM_000406.3:c.413A>T MANE Select	NP_000397.1:p.Asp138Val
NM_001012763.2:c.413A>T	NP_001012781.1:p.Asp138Val