Canonical Allele Identifier: CA1248761620

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48983125G= , CM000664.2:g.48983125G=	GRCh38
NC_000002.11:g.49210264G= , CM000664.1:g.49210264G=	GRCh37
NC_000002.10:g.49063768G=	NCBI36
NG_008146.1:g.176367C= , LRG_536:g.176367C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.566C= MANE Select	ENSP00000384708.2:p.Ala189=
ENST00000304421.8:c.488C=	ENSP00000306780.4:p.Ala163=
ENST00000406846.6:c.566C=	ENSP00000384708.2:p.Ala189=
ENST00000419927.1:c.*358C=	ENSP00000405775.1:n.*358C=
ENST00000454032.5:c.566C=	ENSP00000415504.1:p.Ala189=
ENST00000469138.5:n.327C=
NM_000145.3:c.566C= , LRG_536t1:c.566C=	NP_000136.2:p.Ala189=
NM_181446.2:c.488C=	NP_852111.2:p.Ala163=
XM_011532733.1:c.566C=	XP_011531035.1:p.Ala189=
XM_011532734.1:c.233C=	XP_011531036.1:p.Ala78=
XM_011532735.1:c.-329C=	XP_011531037.1:n.-329C=
XM_011532736.1:c.-227C=	XP_011531038.1:n.-227C=
XM_011532737.1:c.566C=	XP_011531039.1:p.Ala189=
XM_011532738.1:c.566C=	XP_011531040.1:p.Ala189=
XM_011532739.1:c.566C=	XP_011531041.1:p.Ala189=
XM_011532740.1:c.566C=	XP_011531042.1:p.Ala189=
XM_011532733.2:c.566C=	XP_011531035.1:p.Ala189=
XM_011532734.2:c.233C=	XP_011531036.1:p.Ala78=
XM_011532735.2:c.-329C=	XP_011531037.1:n.-329C=
XM_011532736.2:c.-227C=	XP_011531038.1:n.-227C=
NM_000145.4:c.566C= MANE Select	NP_000136.2:p.Ala189=
NM_181446.3:c.488C=	NP_852111.2:p.Ala163=