Canonical Allele Identifier: CA646958486

Gene: FSHR

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154446_49154447insT , CM000664.2:g.49154446_49154447insT	GRCh38
NC_000002.11:g.49381585_49381586insT , CM000664.1:g.49381585_49381586insT	GRCh37
NC_000002.10:g.49235089_49235090insT	NCBI36
NG_008146.1:g.5045_5046insA , LRG_536:g.5045_5046insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.-30_-29insA MANE Select	ENSP00000384708.2:n.-30_-29insA
ENST00000304421.8:c.-30_-29insA	ENSP00000306780.4:n.-30_-29insA
ENST00000406846.6:c.-30_-29insA	ENSP00000384708.2:n.-30_-29insA
ENST00000419927.1:c.-30_-29insA	ENSP00000405775.1:n.-30_-29insA
NM_000145.3:c.-30_-29insA , LRG_536t1:c.-30_-29insA	NP_000136.2:n.-30_-29insA
NM_181446.2:c.-30_-29insA	NP_852111.2:n.-30_-29insA
XM_011532733.1:c.-30_-29insA	XP_011531035.1:n.-30_-29insA
XM_011532734.1:c.-614_-613insA	XP_011531036.1:n.-614_-613insA
XM_011532737.1:c.-30_-29insA	XP_011531039.1:n.-30_-29insA
XM_011532738.1:c.-30_-29insA	XP_011531040.1:n.-30_-29insA
XM_011532739.1:c.-30_-29insA	XP_011531041.1:n.-30_-29insA
XM_011532740.1:c.-30_-29insA	XP_011531042.1:n.-30_-29insA
XM_011532733.2:c.-30_-29insA	XP_011531035.1:n.-30_-29insA
XM_011532734.2:c.-614_-613insA	XP_011531036.1:n.-614_-613insA
NM_000145.4:c.-30_-29insA MANE Select	NP_000136.2:n.-30_-29insA
NM_181446.3:c.-30_-29insA	NP_852111.2:n.-30_-29insA