Canonical Allele Identifier: CA357047642

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606316T>A (hg19) ; chr4:g.67740598T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740598T>A , CM000666.2:g.67740598T>A	GRCh38
NC_000004.11:g.68606316T>A , CM000666.1:g.68606316T>A	GRCh37
NC_000004.10:g.68288911T>A	NCBI36
NG_009293.1:g.20489A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.869A>T MANE Select	ENSP00000226413.5:p.Tyr290Phe
ENST00000226413.4:c.869A>T	ENSP00000226413.4:p.Tyr290Phe
ENST00000420975.2:c.741A>T	ENSP00000397561.2:p.Val247=
NM_000406.2:c.869A>T	NP_000397.1:p.Tyr290Phe
NM_001012763.1:c.741A>T	NP_001012781.1:p.Val247=
NM_000406.3:c.869A>T MANE Select	NP_000397.1:p.Tyr290Phe
NM_001012763.2:c.741A>T	NP_001012781.1:p.Val247=