Canonical Allele Identifier: CA1248856500

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154466C= , CM000664.2:g.49154466C=	GRCh38
NC_000002.11:g.49381605C= , CM000664.1:g.49381605C=	GRCh37
NC_000002.10:g.49235109C=	NCBI36
NG_008146.1:g.5026G= , LRG_536:g.5026G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000406846.7:c.-49G= MANE Select	ENSP00000384708.2:n.-49G=
ENST00000304421.8:c.-49G=	ENSP00000306780.4:n.-49G=
ENST00000406846.6:c.-49G=	ENSP00000384708.2:n.-49G=
ENST00000419927.1:c.-49G=	ENSP00000405775.1:n.-49G=
NM_000145.3:c.-49G= , LRG_536t1:c.-49G=	NP_000136.2:n.-49G=
NM_181446.2:c.-49G=	NP_852111.2:n.-49G=
XM_011532733.1:c.-49G=	XP_011531035.1:n.-49G=
XM_011532734.1:c.-633G=	XP_011531036.1:n.-633G=
XM_011532737.1:c.-49G=	XP_011531039.1:n.-49G=
XM_011532738.1:c.-49G=	XP_011531040.1:n.-49G=
XM_011532739.1:c.-49G=	XP_011531041.1:n.-49G=
XM_011532740.1:c.-49G=	XP_011531042.1:n.-49G=
XM_011532733.2:c.-49G=	XP_011531035.1:n.-49G=
XM_011532734.2:c.-633G=	XP_011531036.1:n.-633G=
NM_000145.4:c.-49G= MANE Select	NP_000136.2:n.-49G=
NM_181446.3:c.-49G=	NP_852111.2:n.-49G=