Canonical Allele Identifier: CA1248756912

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48974473C= , CM000664.2:g.48974473C=	GRCh38
NC_000002.11:g.49201612C= , CM000664.1:g.49201612C=	GRCh37
NC_000002.10:g.49055116C=	NCBI36
NG_008146.1:g.185019G= , LRG_536:g.185019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.669-5590G= MANE Select	ENSP00000384708.2:n.669-5590G=
ENST00000304421.8:c.591-5590G=	ENSP00000306780.4:n.591-5590G=
ENST00000406846.6:c.669-5590G=	ENSP00000384708.2:n.669-5590G=
ENST00000454032.5:c.668+8439G=	ENSP00000415504.1:n.668+8439G=
ENST00000469138.5:n.430-5590G=
NM_000145.3:c.669-5590G= , LRG_536t1:c.669-5590G=	NP_000136.2:n.669-5590G=
NM_181446.2:c.591-5590G=	NP_852111.2:n.591-5590G=
XM_011532733.1:c.669-5387G=	XP_011531035.1:n.669-5387G=
XM_011532734.1:c.336-5387G=	XP_011531036.1:n.336-5387G=
XM_011532735.1:c.-226-5387G=	XP_011531037.1:n.-226-5387G=
XM_011532736.1:c.-124-5590G=	XP_011531038.1:n.-124-5590G=
XM_011532737.1:c.669-5387G=	XP_011531039.1:n.669-5387G=
XM_011532738.1:c.669-5387G=	XP_011531040.1:n.669-5387G=
XM_011532739.1:c.669-5387G=	XP_011531041.1:n.669-5387G=
XM_011532740.1:c.669-5387G=	XP_011531042.1:n.669-5387G=
XM_011532733.2:c.669-5387G=	XP_011531035.1:n.669-5387G=
XM_011532734.2:c.336-5387G=	XP_011531036.1:n.336-5387G=
XM_011532735.2:c.-226-5387G=	XP_011531037.1:n.-226-5387G=
XM_011532736.2:c.-124-5590G=	XP_011531038.1:n.-124-5590G=
NM_000145.4:c.669-5590G= MANE Select	NP_000136.2:n.669-5590G=
NM_181446.3:c.591-5590G=	NP_852111.2:n.591-5590G=