Canonical Allele Identifier: CA1248751311

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963778G= , CM000664.2:g.48963778G=	GRCh38
NC_000002.11:g.49190917G= , CM000664.1:g.49190917G=	GRCh37
NC_000002.10:g.49044421G=	NCBI36
NG_008146.1:g.195714C= , LRG_536:g.195714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1043C= MANE Select	ENSP00000384708.2:p.Pro348=
ENST00000304421.8:c.965C=	ENSP00000306780.4:p.Pro322=
ENST00000406846.6:c.1043C=	ENSP00000384708.2:p.Pro348=
NM_000145.3:c.1043C= , LRG_536t1:c.1043C=	NP_000136.2:p.Pro348=
NM_181446.2:c.965C=	NP_852111.2:p.Pro322=
XM_011532733.1:c.1145C=	XP_011531035.1:p.Pro382=
XM_011532734.1:c.812C=	XP_011531036.1:p.Pro271=
XM_011532735.1:c.251C=	XP_011531037.1:p.Pro84=
XM_011532736.1:c.251C=	XP_011531038.1:p.Pro84=
XM_011532737.1:c.956+4920C=	XP_011531039.1:n.956+4920C=
XM_011532738.1:c.956+4920C=	XP_011531040.1:n.956+4920C=
XM_011532739.1:c.956+4920C=	XP_011531041.1:n.956+4920C=
XM_011532733.2:c.1145C=	XP_011531035.1:p.Pro382=
XM_011532734.2:c.812C=	XP_011531036.1:p.Pro271=
XM_011532735.2:c.251C=	XP_011531037.1:p.Pro84=
XM_011532736.2:c.251C=	XP_011531038.1:p.Pro84=
NM_000145.4:c.1043C= MANE Select	NP_000136.2:p.Pro348=
NM_181446.3:c.965C=	NP_852111.2:p.Pro322=