Canonical Allele Identifier: CA357047625

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606312C>A (hg19) ; chr4:g.67740594C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740594C>A , CM000666.2:g.67740594C>A	GRCh38
NC_000004.11:g.68606312C>A , CM000666.1:g.68606312C>A	GRCh37
NC_000004.10:g.68288907C>A	NCBI36
NG_009293.1:g.20493G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.873G>T MANE Select	ENSP00000226413.5:p.Trp291Cys
ENST00000226413.4:c.873G>T	ENSP00000226413.4:p.Trp291Cys
ENST00000420975.2:c.745G>T	ENSP00000397561.2:p.Val249Phe
NM_000406.2:c.873G>T	NP_000397.1:p.Trp291Cys
NM_001012763.1:c.745G>T	NP_001012781.1:p.Val249Phe
NM_000406.3:c.873G>T MANE Select	NP_000397.1:p.Trp291Cys
NM_001012763.2:c.745G>T	NP_001012781.1:p.Val249Phe