Canonical Allele Identifier: CA1248750857

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48962782C= , CM000664.2:g.48962782C=	GRCh38
NC_000002.11:g.49189921C= , CM000664.1:g.49189921C=	GRCh37
NC_000002.10:g.49043425C=	NCBI36
NG_008146.1:g.196710G= , LRG_536:g.196710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.2039G= MANE Select	ENSP00000384708.2:p.Ser680=
ENST00000304421.8:c.1961G=	ENSP00000306780.4:p.Ser654=
ENST00000406846.6:c.2039G=	ENSP00000384708.2:p.Ser680=
NM_000145.3:c.2039G= , LRG_536t1:c.2039G=	NP_000136.2:p.Ser680=
NM_181446.2:c.1961G=	NP_852111.2:p.Ser654=
XM_011532733.1:c.2141G=	XP_011531035.1:p.Ser714=
XM_011532734.1:c.1808G=	XP_011531036.1:p.Ser603=
XM_011532735.1:c.1247G=	XP_011531037.1:p.Ser416=
XM_011532736.1:c.1247G=	XP_011531038.1:p.Ser416=
XM_011532737.1:c.956+5916G=	XP_011531039.1:n.956+5916G=
XM_011532738.1:c.956+5916G=	XP_011531040.1:n.956+5916G=
XM_011532739.1:c.956+5916G=	XP_011531041.1:n.956+5916G=
XM_011532733.2:c.2141G=	XP_011531035.1:p.Ser714=
XM_011532734.2:c.1808G=	XP_011531036.1:p.Ser603=
XM_011532735.2:c.1247G=	XP_011531037.1:p.Ser416=
XM_011532736.2:c.1247G=	XP_011531038.1:p.Ser416=
NM_000145.4:c.2039G= MANE Select	NP_000136.2:p.Ser680=
NM_181446.3:c.1961G=	NP_852111.2:p.Ser654=