Canonical Allele Identifier: CA1248751380

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963902C= , CM000664.2:g.48963902C=	GRCh38
NC_000002.11:g.49191041C= , CM000664.1:g.49191041C=	GRCh37
NC_000002.10:g.49044545C=	NCBI36
NG_008146.1:g.195590G= , LRG_536:g.195590G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000145.4:c.919G= MANE Select	NP_000136.2:p.Ala307=
ENST00000406846.7:c.919G= MANE Select	ENSP00000384708.2:p.Ala307=
NM_000145.3:c.919G= , LRG_536t1:c.919G=	NP_000136.2:p.Ala307=
NM_181446.2:c.841G=	NP_852111.2:p.Ala281=
NM_181446.3:c.841G=	NP_852111.2:p.Ala281=
ENST00000304421.8:c.841G=	ENSP00000306780.4:p.Ala281=
ENST00000406846.6:c.919G=	ENSP00000384708.2:p.Ala307=
ENST00000454032.5:c.733G=	ENSP00000415504.1:p.Ala245=
XM_011532733.1:c.1021G=	XP_011531035.1:p.Ala341=
XM_011532733.2:c.1021G=	XP_011531035.1:p.Ala341=
XM_011532734.1:c.688G=	XP_011531036.1:p.Ala230=
XM_011532734.2:c.688G=	XP_011531036.1:p.Ala230=
XM_011532735.1:c.127G=	XP_011531037.1:p.Ala43=
XM_011532735.2:c.127G=	XP_011531037.1:p.Ala43=
XM_011532736.1:c.127G=	XP_011531038.1:p.Ala43=
XM_011532736.2:c.127G=	XP_011531038.1:p.Ala43=
XM_011532737.1:c.956+4796G=	XP_011531039.1:n.956+4796G=
XM_011532738.1:c.956+4796G=	XP_011531040.1:n.956+4796G=
XM_011532739.1:c.956+4796G=	XP_011531041.1:n.956+4796G=