Canonical Allele Identifier: CA1248753969

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48968881T= , CM000664.2:g.48968881T=	GRCh38
NC_000002.11:g.49196020T= , CM000664.1:g.49196020T=	GRCh37
NC_000002.10:g.49049524T=	NCBI36
NG_008146.1:g.190611A= , LRG_536:g.190611A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.671A= MANE Select	ENSP00000384708.2:p.Asp224=
ENST00000304421.8:c.593A=	ENSP00000306780.4:p.Asp198=
ENST00000406846.6:c.671A=	ENSP00000384708.2:p.Asp224=
ENST00000454032.5:c.669-4915A=	ENSP00000415504.1:n.669-4915A=
ENST00000469138.5:n.432A=
NM_000145.3:c.671A= , LRG_536t1:c.671A=	NP_000136.2:p.Asp224=
NM_181446.2:c.593A=	NP_852111.2:p.Asp198=
XM_011532733.1:c.773A=	XP_011531035.1:p.Asp258=
XM_011532734.1:c.440A=	XP_011531036.1:p.Asp147=
XM_011532735.1:c.-122A=	XP_011531037.1:n.-122A=
XM_011532736.1:c.-122A=	XP_011531038.1:n.-122A=
XM_011532737.1:c.773A=	XP_011531039.1:p.Asp258=
XM_011532738.1:c.773A=	XP_011531040.1:p.Asp258=
XM_011532739.1:c.773A=	XP_011531041.1:p.Asp258=
XM_011532740.1:c.773A=	XP_011531042.1:p.Asp258=
XM_011532733.2:c.773A=	XP_011531035.1:p.Asp258=
XM_011532734.2:c.440A=	XP_011531036.1:p.Asp147=
XM_011532735.2:c.-122A=	XP_011531037.1:n.-122A=
XM_011532736.2:c.-122A=	XP_011531038.1:n.-122A=
NM_000145.4:c.671A= MANE Select	NP_000136.2:p.Asp224=
NM_181446.3:c.593A=	NP_852111.2:p.Asp198=