Canonical Allele Identifier: CA2658999275

Gene: FSHR

Linked Data

• gnomAD v4: 2-49154468-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154470del , CM000664.2:g.49154470del	GRCh38
NC_000002.11:g.49381609del , CM000664.1:g.49381609del	GRCh37
NC_000002.10:g.49235113del	NCBI36
NG_008146.1:g.5023del , LRG_536:g.5023del

Transcript Alleles

HGVS	Amino-acid change
ENST00000406846.7:c.-52del MANE Select	ENSP00000384708.2:n.-52del
ENST00000304421.8:c.-52del	ENSP00000306780.4:n.-52del
ENST00000406846.6:c.-52del	ENSP00000384708.2:n.-52del
ENST00000419927.1:c.-52del	ENSP00000405775.1:n.-52del
NM_000145.3:c.-52del , LRG_536t1:c.-52del	NP_000136.2:n.-52del
NM_181446.2:c.-52del	NP_852111.2:n.-52del
XM_011532733.1:c.-52del	XP_011531035.1:n.-52del
XM_011532734.1:c.-636del	XP_011531036.1:n.-636del
XM_011532737.1:c.-52del	XP_011531039.1:n.-52del
XM_011532738.1:c.-52del	XP_011531040.1:n.-52del
XM_011532739.1:c.-52del	XP_011531041.1:n.-52del
XM_011532740.1:c.-52del	XP_011531042.1:n.-52del
XM_011532733.2:c.-52del	XP_011531035.1:n.-52del
XM_011532734.2:c.-636del	XP_011531036.1:n.-636del
NM_000145.4:c.-52del MANE Select	NP_000136.2:n.-52del
NM_181446.3:c.-52del	NP_852111.2:n.-52del