Canonical Allele Identifier: CA1248751003

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963104G= , CM000664.2:g.48963104G=	GRCh38
NC_000002.11:g.49190243G= , CM000664.1:g.49190243G=	GRCh37
NC_000002.10:g.49043747G=	NCBI36
NG_008146.1:g.196388C= , LRG_536:g.196388C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1717C= MANE Select	ENSP00000384708.2:p.Arg573=
ENST00000304421.8:c.1639C=	ENSP00000306780.4:p.Arg547=
ENST00000406846.6:c.1717C=	ENSP00000384708.2:p.Arg573=
NM_000145.3:c.1717C= , LRG_536t1:c.1717C=	NP_000136.2:p.Arg573=
NM_181446.2:c.1639C=	NP_852111.2:p.Arg547=
XM_011532733.1:c.1819C=	XP_011531035.1:p.Arg607=
XM_011532734.1:c.1486C=	XP_011531036.1:p.Arg496=
XM_011532735.1:c.925C=	XP_011531037.1:p.Arg309=
XM_011532736.1:c.925C=	XP_011531038.1:p.Arg309=
XM_011532737.1:c.956+5594C=	XP_011531039.1:n.956+5594C=
XM_011532738.1:c.956+5594C=	XP_011531040.1:n.956+5594C=
XM_011532739.1:c.956+5594C=	XP_011531041.1:n.956+5594C=
XM_011532733.2:c.1819C=	XP_011531035.1:p.Arg607=
XM_011532734.2:c.1486C=	XP_011531036.1:p.Arg496=
XM_011532735.2:c.925C=	XP_011531037.1:p.Arg309=
XM_011532736.2:c.925C=	XP_011531038.1:p.Arg309=
NM_000145.4:c.1717C= MANE Select	NP_000136.2:p.Arg573=
NM_181446.3:c.1639C=	NP_852111.2:p.Arg547=