Canonical Allele Identifier: CA1248761481
Gene: FSHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48982829A= , CM000664.2:g.48982829A= GRCh38
NC_000002.11:g.49209968A= , CM000664.1:g.49209968A= GRCh37
NC_000002.10:g.49063472A= NCBI36
NG_008146.1:g.176663T= , LRG_536:g.176663T=

Transcript Alleles

HGVS Amino-acid change
ENST00000406846.7:c.668+83T= MANE Select ENSP00000384708.2:n.668+83T=
ENST00000304421.8:c.590+83T= ENSP00000306780.4:n.590+83T=
ENST00000406846.6:c.668+83T= ENSP00000384708.2:n.668+83T=
ENST00000454032.5:c.668+83T= ENSP00000415504.1:n.668+83T=
ENST00000469138.5:n.429+83T=
NM_000145.3:c.668+83T= , LRG_536t1:c.668+83T= NP_000136.2:n.668+83T=
NM_181446.2:c.590+83T= NP_852111.2:n.590+83T=
XM_011532733.1:c.668+83T= XP_011531035.1:n.668+83T=
XM_011532734.1:c.335+83T= XP_011531036.1:n.335+83T=
XM_011532735.1:c.-227+83T= XP_011531037.1:n.-227+83T=
XM_011532736.1:c.-125+83T= XP_011531038.1:n.-125+83T=
XM_011532737.1:c.668+83T= XP_011531039.1:n.668+83T=
XM_011532738.1:c.668+83T= XP_011531040.1:n.668+83T=
XM_011532739.1:c.668+83T= XP_011531041.1:n.668+83T=
XM_011532740.1:c.668+83T= XP_011531042.1:n.668+83T=
XM_011532733.2:c.668+83T= XP_011531035.1:n.668+83T=
XM_011532734.2:c.335+83T= XP_011531036.1:n.335+83T=
XM_011532735.2:c.-227+83T= XP_011531037.1:n.-227+83T=
XM_011532736.2:c.-125+83T= XP_011531038.1:n.-125+83T=
NM_000145.4:c.668+83T= MANE Select NP_000136.2:n.668+83T=
NM_181446.3:c.590+83T= NP_852111.2:n.590+83T=