Canonical Allele Identifier: CA1248856498

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154465_49154468delinsACCT , CM000664.2:g.49154465_49154468delinsACCT	GRCh38
NC_000002.11:g.49381604_49381607delinsACCT , CM000664.1:g.49381604_49381607delinsACCT	GRCh37
NC_000002.10:g.49235108_49235111delinsACCT	NCBI36
NG_008146.1:g.5024_5027delinsAGGT , LRG_536:g.5024_5027delinsAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.-51_-48delinsAGGT MANE Select	ENSP00000384708.2:n.-51_-48delinsAGGT
ENST00000304421.8:c.-51_-48delinsAGGT	ENSP00000306780.4:n.-51_-48delinsAGGT
ENST00000406846.6:c.-51_-48delinsAGGT	ENSP00000384708.2:n.-51_-48delinsAGGT
ENST00000419927.1:c.-51_-48delinsAGGT	ENSP00000405775.1:n.-51_-48delinsAGGT
NM_000145.3:c.-51_-48delinsAGGT , LRG_536t1:c.-51_-48delinsAGGT	NP_000136.2:n.-51_-48delinsAGGT
NM_181446.2:c.-51_-48delinsAGGT	NP_852111.2:n.-51_-48delinsAGGT
XM_011532733.1:c.-51_-48delinsAGGT	XP_011531035.1:n.-51_-48delinsAGGT
XM_011532734.1:c.-635_-632delinsAGGT	XP_011531036.1:n.-635_-632delinsAGGT
XM_011532737.1:c.-51_-48delinsAGGT	XP_011531039.1:n.-51_-48delinsAGGT
XM_011532738.1:c.-51_-48delinsAGGT	XP_011531040.1:n.-51_-48delinsAGGT
XM_011532739.1:c.-51_-48delinsAGGT	XP_011531041.1:n.-51_-48delinsAGGT
XM_011532740.1:c.-51_-48delinsAGGT	XP_011531042.1:n.-51_-48delinsAGGT
XM_011532733.2:c.-51_-48delinsAGGT	XP_011531035.1:n.-51_-48delinsAGGT
XM_011532734.2:c.-635_-632delinsAGGT	XP_011531036.1:n.-635_-632delinsAGGT
NM_000145.4:c.-51_-48delinsAGGT MANE Select	NP_000136.2:n.-51_-48delinsAGGT
NM_181446.3:c.-51_-48delinsAGGT	NP_852111.2:n.-51_-48delinsAGGT