Canonical Allele Identifier: CA2580585776

Gene: FSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154446C>A , CM000664.2:g.49154446C>A	GRCh38
NC_000002.11:g.49381585C>A , CM000664.1:g.49381585C>A	GRCh37
NC_000002.10:g.49235089C>A	NCBI36
NG_008146.1:g.5046G>T , LRG_536:g.5046G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.-29G>T MANE Select	ENSP00000384708.2:n.-29G>T
ENST00000304421.8:c.-29G>T	ENSP00000306780.4:n.-29G>T
ENST00000406846.6:c.-29G>T	ENSP00000384708.2:n.-29G>T
ENST00000419927.1:c.-29G>T	ENSP00000405775.1:n.-29G>T
NM_000145.3:c.-29G>T , LRG_536t1:c.-29G>T	NP_000136.2:n.-29G>T
NM_181446.2:c.-29G>T	NP_852111.2:n.-29G>T
XM_011532733.1:c.-29G>T	XP_011531035.1:n.-29G>T
XM_011532734.1:c.-613G>T	XP_011531036.1:n.-613G>T
XM_011532737.1:c.-29G>T	XP_011531039.1:n.-29G>T
XM_011532738.1:c.-29G>T	XP_011531040.1:n.-29G>T
XM_011532739.1:c.-29G>T	XP_011531041.1:n.-29G>T
XM_011532740.1:c.-29G>T	XP_011531042.1:n.-29G>T
XM_011532733.2:c.-29G>T	XP_011531035.1:n.-29G>T
XM_011532734.2:c.-613G>T	XP_011531036.1:n.-613G>T
NM_000145.4:c.-29G>T MANE Select	NP_000136.2:n.-29G>T
NM_181446.3:c.-29G>T	NP_852111.2:n.-29G>T