Canonical Allele Identifier: CA1248856433

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154357G= , CM000664.2:g.49154357G=	GRCh38
NC_000002.11:g.49381496G= , CM000664.1:g.49381496G=	GRCh37
NC_000002.10:g.49235000G=	NCBI36
NG_008146.1:g.5135C= , LRG_536:g.5135C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.61C= MANE Select	ENSP00000384708.2:p.Arg21=
ENST00000304421.8:c.61C=	ENSP00000306780.4:p.Arg21=
ENST00000406846.6:c.61C=	ENSP00000384708.2:p.Arg21=
ENST00000419927.1:c.61C=	ENSP00000405775.1:p.Arg21=
ENST00000454032.5:c.61C=	ENSP00000415504.1:p.Arg21=
NM_000145.3:c.61C= , LRG_536t1:c.61C=	NP_000136.2:p.Arg21=
NM_181446.2:c.61C=	NP_852111.2:p.Arg21=
XM_011532733.1:c.61C=	XP_011531035.1:p.Arg21=
XM_011532734.1:c.-524C=	XP_011531036.1:n.-524C=
XM_011532737.1:c.61C=	XP_011531039.1:p.Arg21=
XM_011532738.1:c.61C=	XP_011531040.1:p.Arg21=
XM_011532739.1:c.61C=	XP_011531041.1:p.Arg21=
XM_011532740.1:c.61C=	XP_011531042.1:p.Arg21=
XM_011532733.2:c.61C=	XP_011531035.1:p.Arg21=
XM_011532734.2:c.-524C=	XP_011531036.1:n.-524C=
NM_000145.4:c.61C= MANE Select	NP_000136.2:p.Arg21=
NM_181446.3:c.61C=	NP_852111.2:p.Arg21=