Canonical Allele Identifier: CA1248751086

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48963266G= , CM000664.2:g.48963266G=	GRCh38
NC_000002.11:g.49190405G= , CM000664.1:g.49190405G=	GRCh37
NC_000002.10:g.49043909G=	NCBI36
NG_008146.1:g.196226C= , LRG_536:g.196226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.1555C= MANE Select	ENSP00000384708.2:p.Pro519=
ENST00000304421.8:c.1477C=	ENSP00000306780.4:p.Pro493=
ENST00000406846.6:c.1555C=	ENSP00000384708.2:p.Pro519=
NM_000145.3:c.1555C= , LRG_536t1:c.1555C=	NP_000136.2:p.Pro519=
NM_181446.2:c.1477C=	NP_852111.2:p.Pro493=
XM_011532733.1:c.1657C=	XP_011531035.1:p.Pro553=
XM_011532734.1:c.1324C=	XP_011531036.1:p.Pro442=
XM_011532735.1:c.763C=	XP_011531037.1:p.Pro255=
XM_011532736.1:c.763C=	XP_011531038.1:p.Pro255=
XM_011532737.1:c.956+5432C=	XP_011531039.1:n.956+5432C=
XM_011532738.1:c.956+5432C=	XP_011531040.1:n.956+5432C=
XM_011532739.1:c.956+5432C=	XP_011531041.1:n.956+5432C=
XM_011532733.2:c.1657C=	XP_011531035.1:p.Pro553=
XM_011532734.2:c.1324C=	XP_011531036.1:p.Pro442=
XM_011532735.2:c.763C=	XP_011531037.1:p.Pro255=
XM_011532736.2:c.763C=	XP_011531038.1:p.Pro255=
NM_000145.4:c.1555C= MANE Select	NP_000136.2:p.Pro519=
NM_181446.3:c.1477C=	NP_852111.2:p.Pro493=