Canonical Allele Identifier: CA1248750969

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963029T= , CM000664.2:g.48963029T=	GRCh38
NC_000002.11:g.49190168T= , CM000664.1:g.49190168T=	GRCh37
NC_000002.10:g.49043672T=	NCBI36
NG_008146.1:g.196463A= , LRG_536:g.196463A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1792A= MANE Select	ENSP00000384708.2:p.Lys598=
ENST00000304421.8:c.1714A=	ENSP00000306780.4:p.Lys572=
ENST00000406846.6:c.1792A=	ENSP00000384708.2:p.Lys598=
NM_000145.3:c.1792A= , LRG_536t1:c.1792A=	NP_000136.2:p.Lys598=
NM_181446.2:c.1714A=	NP_852111.2:p.Lys572=
XM_011532733.1:c.1894A=	XP_011531035.1:p.Lys632=
XM_011532734.1:c.1561A=	XP_011531036.1:p.Lys521=
XM_011532735.1:c.1000A=	XP_011531037.1:p.Lys334=
XM_011532736.1:c.1000A=	XP_011531038.1:p.Lys334=
XM_011532737.1:c.956+5669A=	XP_011531039.1:n.956+5669A=
XM_011532738.1:c.956+5669A=	XP_011531040.1:n.956+5669A=
XM_011532739.1:c.956+5669A=	XP_011531041.1:n.956+5669A=
XM_011532733.2:c.1894A=	XP_011531035.1:p.Lys632=
XM_011532734.2:c.1561A=	XP_011531036.1:p.Lys521=
XM_011532735.2:c.1000A=	XP_011531037.1:p.Lys334=
XM_011532736.2:c.1000A=	XP_011531038.1:p.Lys334=
NM_000145.4:c.1792A= MANE Select	NP_000136.2:p.Lys598=
NM_181446.3:c.1714A=	NP_852111.2:p.Lys572=