Canonical Allele Identifier: CA1248751179

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963475G= , CM000664.2:g.48963475G=	GRCh38
NC_000002.11:g.49190614G= , CM000664.1:g.49190614G=	GRCh37
NC_000002.10:g.49044118G=	NCBI36
NG_008146.1:g.196017C= , LRG_536:g.196017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1346C= MANE Select	ENSP00000384708.2:p.Thr449=
ENST00000304421.8:c.1268C=	ENSP00000306780.4:p.Thr423=
ENST00000406846.6:c.1346C=	ENSP00000384708.2:p.Thr449=
NM_000145.3:c.1346C= , LRG_536t1:c.1346C=	NP_000136.2:p.Thr449=
NM_181446.2:c.1268C=	NP_852111.2:p.Thr423=
XM_011532733.1:c.1448C=	XP_011531035.1:p.Thr483=
XM_011532734.1:c.1115C=	XP_011531036.1:p.Thr372=
XM_011532735.1:c.554C=	XP_011531037.1:p.Thr185=
XM_011532736.1:c.554C=	XP_011531038.1:p.Thr185=
XM_011532737.1:c.956+5223C=	XP_011531039.1:n.956+5223C=
XM_011532738.1:c.956+5223C=	XP_011531040.1:n.956+5223C=
XM_011532739.1:c.956+5223C=	XP_011531041.1:n.956+5223C=
XM_011532733.2:c.1448C=	XP_011531035.1:p.Thr483=
XM_011532734.2:c.1115C=	XP_011531036.1:p.Thr372=
XM_011532735.2:c.554C=	XP_011531037.1:p.Thr185=
XM_011532736.2:c.554C=	XP_011531038.1:p.Thr185=
NM_000145.4:c.1346C= MANE Select	NP_000136.2:p.Thr449=
NM_181446.3:c.1268C=	NP_852111.2:p.Thr423=