Canonical Allele Identifier: CA1248751218

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963566C= , CM000664.2:g.48963566C=	GRCh38
NC_000002.11:g.49190705C= , CM000664.1:g.49190705C=	GRCh37
NC_000002.10:g.49044209C=	NCBI36
NG_008146.1:g.195926G= , LRG_536:g.195926G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000145.4:c.1255G= MANE Select	NP_000136.2:p.Ala419=
ENST00000406846.7:c.1255G= MANE Select	ENSP00000384708.2:p.Ala419=
NM_000145.3:c.1255G= , LRG_536t1:c.1255G=	NP_000136.2:p.Ala419=
NM_181446.2:c.1177G=	NP_852111.2:p.Ala393=
NM_181446.3:c.1177G=	NP_852111.2:p.Ala393=
ENST00000304421.8:c.1177G=	ENSP00000306780.4:p.Ala393=
ENST00000406846.6:c.1255G=	ENSP00000384708.2:p.Ala419=
XM_011532733.1:c.1357G=	XP_011531035.1:p.Ala453=
XM_011532733.2:c.1357G=	XP_011531035.1:p.Ala453=
XM_011532734.1:c.1024G=	XP_011531036.1:p.Ala342=
XM_011532734.2:c.1024G=	XP_011531036.1:p.Ala342=
XM_011532735.1:c.463G=	XP_011531037.1:p.Ala155=
XM_011532735.2:c.463G=	XP_011531037.1:p.Ala155=
XM_011532736.1:c.463G=	XP_011531038.1:p.Ala155=
XM_011532736.2:c.463G=	XP_011531038.1:p.Ala155=
XM_011532737.1:c.956+5132G=	XP_011531039.1:n.956+5132G=
XM_011532738.1:c.956+5132G=	XP_011531040.1:n.956+5132G=
XM_011532739.1:c.956+5132G=	XP_011531041.1:n.956+5132G=