Canonical Allele Identifier: CA1248780779

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49017420A= , CM000664.2:g.49017420A=	GRCh38
NC_000002.11:g.49244559A= , CM000664.1:g.49244559A=	GRCh37
NC_000002.10:g.49098063A=	NCBI36
NG_008146.1:g.142072T= , LRG_536:g.142072T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000145.4:c.374+69T= MANE Select	NP_000136.2:n.374+69T=
ENST00000406846.7:c.374+69T= MANE Select	ENSP00000384708.2:n.374+69T=
NM_000145.3:c.374+69T= , LRG_536t1:c.374+69T=	NP_000136.2:n.374+69T=
NM_181446.2:c.374+69T=	NP_852111.2:n.374+69T=
NM_181446.3:c.374+69T=	NP_852111.2:n.374+69T=
ENST00000304421.8:c.374+69T=	ENSP00000306780.4:n.374+69T=
ENST00000406846.6:c.374+69T=	ENSP00000384708.2:n.374+69T=
ENST00000419927.1:c.374+69T=	ENSP00000405775.1:n.374+69T=
ENST00000454032.5:c.374+69T=	ENSP00000415504.1:n.374+69T=
XM_011532733.1:c.374+69T=	XP_011531035.1:n.374+69T=
XM_011532733.2:c.374+69T=	XP_011531035.1:n.374+69T=
XM_011532734.1:c.-211+69T=	XP_011531036.1:n.-211+69T=
XM_011532734.2:c.-211+69T=	XP_011531036.1:n.-211+69T=
XM_011532737.1:c.374+69T=	XP_011531039.1:n.374+69T=
XM_011532738.1:c.374+69T=	XP_011531040.1:n.374+69T=
XM_011532739.1:c.374+69T=	XP_011531041.1:n.374+69T=
XM_011532740.1:c.374+69T=	XP_011531042.1:n.374+69T=