Canonical Allele Identifier: CA439924279

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606279G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740561G>A , CM000666.2:g.67740561G>A	GRCh38
NC_000004.11:g.68606279G>A , CM000666.1:g.68606279G>A	GRCh37
NC_000004.10:g.68288874G>A	NCBI36
NG_009293.1:g.20526C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.906C>T MANE Select	ENSP00000226413.5:p.Asp302=
ENST00000226413.4:c.906C>T	ENSP00000226413.4:p.Asp302=
ENST00000420975.2:c.778C>T	ENSP00000397561.2:n.778C>T
NM_000406.2:c.906C>T	NP_000397.1:p.Asp302=
NM_001012763.1:c.*28C>T	NP_001012781.1:n.*28C>T
NM_000406.3:c.906C>T MANE Select	NP_000397.1:p.Asp302=
NM_001012763.2:c.*28C>T	NP_001012781.1:n.*28C>T