Canonical Allele Identifier: CA1248764811

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48989022A= , CM000664.2:g.48989022A=	GRCh38
NC_000002.11:g.49216161A= , CM000664.1:g.49216161A=	GRCh37
NC_000002.10:g.49069665A=	NCBI36
NG_008146.1:g.170470T= , LRG_536:g.170470T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.479T= MANE Select	ENSP00000384708.2:p.Ile160=
ENST00000304421.8:c.446+1544T=	ENSP00000306780.4:n.446+1544T=
ENST00000406846.6:c.479T=	ENSP00000384708.2:p.Ile160=
ENST00000419927.1:c.*271T=	ENSP00000405775.1:n.*271T=
ENST00000454032.5:c.479T=	ENSP00000415504.1:p.Ile160=
ENST00000469138.5:n.240T=
NM_000145.3:c.479T= , LRG_536t1:c.479T=	NP_000136.2:p.Ile160=
NM_181446.2:c.446+1544T=	NP_852111.2:n.446+1544T=
XM_011532733.1:c.479T=	XP_011531035.1:p.Ile160=
XM_011532734.1:c.146T=	XP_011531036.1:p.Ile49=
XM_011532735.1:c.-416T=	XP_011531037.1:n.-416T=
XM_011532736.1:c.-314T=	XP_011531038.1:n.-314T=
XM_011532737.1:c.479T=	XP_011531039.1:p.Ile160=
XM_011532738.1:c.479T=	XP_011531040.1:p.Ile160=
XM_011532739.1:c.479T=	XP_011531041.1:p.Ile160=
XM_011532740.1:c.479T=	XP_011531042.1:p.Ile160=
XM_011532733.2:c.479T=	XP_011531035.1:p.Ile160=
XM_011532734.2:c.146T=	XP_011531036.1:p.Ile49=
XM_011532735.2:c.-416T=	XP_011531037.1:n.-416T=
XM_011532736.2:c.-314T=	XP_011531038.1:n.-314T=
NM_000145.4:c.479T= MANE Select	NP_000136.2:p.Ile160=
NM_181446.3:c.446+1544T=	NP_852111.2:n.446+1544T=