Canonical Allele Identifier: CA357048149

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606380T>A (hg19) ; chr4:g.67740662T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740662T>A , CM000666.2:g.67740662T>A	GRCh38
NC_000004.11:g.68606380T>A , CM000666.1:g.68606380T>A	GRCh37
NC_000004.10:g.68288975T>A	NCBI36
NG_009293.1:g.20425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.805A>T MANE Select	ENSP00000226413.5:p.Thr269Ser
ENST00000226413.4:c.805A>T	ENSP00000226413.4:p.Thr269Ser
ENST00000420975.2:c.677A>T	ENSP00000397561.2:p.Asp226Val
NM_000406.2:c.805A>T	NP_000397.1:p.Thr269Ser
NM_001012763.1:c.677A>T	NP_001012781.1:p.Asp226Val
NM_000406.3:c.805A>T MANE Select	NP_000397.1:p.Thr269Ser
NM_001012763.2:c.677A>T	NP_001012781.1:p.Asp226Val