Canonical Allele Identifier: CA346769310

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48968881T>C , CM000664.2:g.48968881T>C	GRCh38
NC_000002.11:g.49196020T>C , CM000664.1:g.49196020T>C	GRCh37
NC_000002.10:g.49049524T>C	NCBI36
NG_008146.1:g.190611A>G , LRG_536:g.190611A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.671A>G MANE Select	ENSP00000384708.2:p.Asp224Gly
ENST00000304421.8:c.593A>G	ENSP00000306780.4:p.Asp198Gly
ENST00000406846.6:c.671A>G	ENSP00000384708.2:p.Asp224Gly
ENST00000454032.5:c.669-4915A>G	ENSP00000415504.1:n.669-4915A>G
ENST00000469138.5:n.432A>G
NM_000145.3:c.671A>G , LRG_536t1:c.671A>G	NP_000136.2:p.Asp224Gly
NM_181446.2:c.593A>G	NP_852111.2:p.Asp198Gly
XM_011532733.1:c.773A>G	XP_011531035.1:p.Asp258Gly
XM_011532734.1:c.440A>G	XP_011531036.1:p.Asp147Gly
XM_011532735.1:c.-122A>G	XP_011531037.1:n.-122A>G
XM_011532736.1:c.-122A>G	XP_011531038.1:n.-122A>G
XM_011532737.1:c.773A>G	XP_011531039.1:p.Asp258Gly
XM_011532738.1:c.773A>G	XP_011531040.1:p.Asp258Gly
XM_011532739.1:c.773A>G	XP_011531041.1:p.Asp258Gly
XM_011532740.1:c.773A>G	XP_011531042.1:p.Asp258Gly
XM_011532733.2:c.773A>G	XP_011531035.1:p.Asp258Gly
XM_011532734.2:c.440A>G	XP_011531036.1:p.Asp147Gly
XM_011532735.2:c.-122A>G	XP_011531037.1:n.-122A>G
XM_011532736.2:c.-122A>G	XP_011531038.1:n.-122A>G
NM_000145.4:c.671A>G MANE Select	NP_000136.2:p.Asp224Gly
NM_181446.3:c.593A>G	NP_852111.2:p.Asp198Gly