Canonical Allele Identifier: CA357047766

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606334T>A (hg19) ; chr4:g.67740616T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740616T>A , CM000666.2:g.67740616T>A	GRCh38
NC_000004.11:g.68606334T>A , CM000666.1:g.68606334T>A	GRCh37
NC_000004.10:g.68288929T>A	NCBI36
NG_009293.1:g.20471A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.851A>T MANE Select	ENSP00000226413.5:p.Tyr284Phe
ENST00000226413.4:c.851A>T	ENSP00000226413.4:p.Tyr284Phe
ENST00000420975.2:c.723A>T	ENSP00000397561.2:p.Leu241=
NM_000406.2:c.851A>T	NP_000397.1:p.Tyr284Phe
NM_001012763.1:c.723A>T	NP_001012781.1:p.Leu241=
NM_000406.3:c.851A>T MANE Select	NP_000397.1:p.Tyr284Phe
NM_001012763.2:c.723A>T	NP_001012781.1:p.Leu241=