Canonical Allele Identifier: CA1248751016

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963126A= , CM000664.2:g.48963126A=	GRCh38
NC_000002.11:g.49190265A= , CM000664.1:g.49190265A=	GRCh37
NC_000002.10:g.49043769A=	NCBI36
NG_008146.1:g.196366T= , LRG_536:g.196366T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1695T= MANE Select	ENSP00000384708.2:p.Ser565=
ENST00000304421.8:c.1617T=	ENSP00000306780.4:p.Ser539=
ENST00000406846.6:c.1695T=	ENSP00000384708.2:p.Ser565=
NM_000145.3:c.1695T= , LRG_536t1:c.1695T=	NP_000136.2:p.Ser565=
NM_181446.2:c.1617T=	NP_852111.2:p.Ser539=
XM_011532733.1:c.1797T=	XP_011531035.1:p.Ser599=
XM_011532734.1:c.1464T=	XP_011531036.1:p.Ser488=
XM_011532735.1:c.903T=	XP_011531037.1:p.Ser301=
XM_011532736.1:c.903T=	XP_011531038.1:p.Ser301=
XM_011532737.1:c.956+5572T=	XP_011531039.1:n.956+5572T=
XM_011532738.1:c.956+5572T=	XP_011531040.1:n.956+5572T=
XM_011532739.1:c.956+5572T=	XP_011531041.1:n.956+5572T=
XM_011532733.2:c.1797T=	XP_011531035.1:p.Ser599=
XM_011532734.2:c.1464T=	XP_011531036.1:p.Ser488=
XM_011532735.2:c.903T=	XP_011531037.1:p.Ser301=
XM_011532736.2:c.903T=	XP_011531038.1:p.Ser301=
NM_000145.4:c.1695T= MANE Select	NP_000136.2:p.Ser565=
NM_181446.3:c.1617T=	NP_852111.2:p.Ser539=