Canonical Allele Identifier: CA11151657

Gene: FSHR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48974473C>T , CM000664.2:g.48974473C>T	GRCh38
NC_000002.11:g.49201612C>T , CM000664.1:g.49201612C>T	GRCh37
NC_000002.10:g.49055116C>T	NCBI36
NG_008146.1:g.185019G>A , LRG_536:g.185019G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.669-5590G>A MANE Select	ENSP00000384708.2:n.669-5590G>A
ENST00000304421.8:c.591-5590G>A	ENSP00000306780.4:n.591-5590G>A
ENST00000406846.6:c.669-5590G>A	ENSP00000384708.2:n.669-5590G>A
ENST00000454032.5:c.668+8439G>A	ENSP00000415504.1:n.668+8439G>A
ENST00000469138.5:n.430-5590G>A
NM_000145.3:c.669-5590G>A , LRG_536t1:c.669-5590G>A	NP_000136.2:n.669-5590G>A
NM_181446.2:c.591-5590G>A	NP_852111.2:n.591-5590G>A
XM_011532733.1:c.669-5387G>A	XP_011531035.1:n.669-5387G>A
XM_011532734.1:c.336-5387G>A	XP_011531036.1:n.336-5387G>A
XM_011532735.1:c.-226-5387G>A	XP_011531037.1:n.-226-5387G>A
XM_011532736.1:c.-124-5590G>A	XP_011531038.1:n.-124-5590G>A
XM_011532737.1:c.669-5387G>A	XP_011531039.1:n.669-5387G>A
XM_011532738.1:c.669-5387G>A	XP_011531040.1:n.669-5387G>A
XM_011532739.1:c.669-5387G>A	XP_011531041.1:n.669-5387G>A
XM_011532740.1:c.669-5387G>A	XP_011531042.1:n.669-5387G>A
XM_011532733.2:c.669-5387G>A	XP_011531035.1:n.669-5387G>A
XM_011532734.2:c.336-5387G>A	XP_011531036.1:n.336-5387G>A
XM_011532735.2:c.-226-5387G>A	XP_011531037.1:n.-226-5387G>A
XM_011532736.2:c.-124-5590G>A	XP_011531038.1:n.-124-5590G>A
NM_000145.4:c.669-5590G>A MANE Select	NP_000136.2:n.669-5590G>A
NM_181446.3:c.591-5590G>A	NP_852111.2:n.591-5590G>A