Canonical Allele Identifier: CA2580061107

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154984050_154984052del , CM000663.2:g.154984050_154984052del	GRCh38
NC_000001.10:g.154956526_154956528del , CM000663.1:g.154956526_154956528del	GRCh37
NC_000001.9:g.153223150_153223152del	NCBI36
NG_042310.1:g.5757_5759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.356_358del MANE Select	ENSP00000292180.3:p.Gly119del
ENST00000292180.7:c.356_358del	ENSP00000292180.3:p.Gly119del
ENST00000315144.14:c.65_67del	ENSP00000317296.10:p.Gly22del
ENST00000368431.7:c.-581_-579del	ENSP00000357416.3:n.-581_-579del
ENST00000368432.5:c.65_67del	ENSP00000357417.1:p.Gly22del
ENST00000368433.5:c.356_358del	ENSP00000357418.1:p.Gly119del
ENST00000487371.1:n.412_414del
ENST00000492620.1:n.60+653_60+655del
NM_001184891.1:c.65_67del	NP_001171820.1:p.Gly22del
NM_001184892.1:c.-581_-579del	NP_001171821.1:n.-581_-579del
NM_025207.4:c.356_358del	NP_079483.3:p.Gly119del
NM_201398.2:c.65_67del	NP_958800.1:p.Gly22del
XM_005245502.2:c.65_67del	XP_005245559.1:p.Gly22del
XM_005245503.2:c.-430+653_-430+655del	XP_005245560.1:n.-430+653_-430+655del
XM_006711559.2:c.65_67del	XP_006711622.1:p.Gly22del
XR_241098.3:n.274_276del
NM_025207.5:c.356_358del MANE Select	NP_079483.3:p.Gly119del
NM_001184891.2:c.65_67del	NP_001171820.1:p.Gly22del
NM_001184892.2:c.-581_-579del	NP_001171821.1:n.-581_-579del
NM_201398.3:c.65_67del	NP_958800.1:p.Gly22del