Canonical Allele Identifier: CA915941443

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154990363_154990372del , CM000663.2:g.154990363_154990372del	GRCh38
NC_000001.10:g.154962839_154962848del , CM000663.1:g.154962839_154962848del	GRCh37
NC_000001.9:g.153229463_153229472del	NCBI36
NG_042310.1:g.12070_12079del

Transcript Alleles

HGVS	Amino-acid Change
NM_025207.5:c.1389_1398del MANE Select	NP_079483.3:p.Glu464Ter
ENST00000292180.8:c.1389_1398del MANE Select	ENSP00000292180.3:p.Glu464Ter
NM_001184891.1:c.1098_1107del	NP_001171820.1:p.Glu367Ter
NM_001184891.2:c.1098_1107del	NP_001171820.1:p.Glu367Ter
NM_025207.4:c.1389_1398del	NP_079483.3:p.Glu464Ter
NM_201398.2:c.1098_1107del	NP_958800.1:p.Glu367Ter
NM_201398.3:c.1098_1107del	NP_958800.1:p.Glu367Ter
ENST00000292180.7:c.1389_1398del	ENSP00000292180.3:p.Glu464Ter
ENST00000295530.6:c.415+106_415+115del	ENSP00000295530.2:n.415+106_415+115del
ENST00000315144.14:c.1098_1107del	ENSP00000317296.10:p.Glu367Ter
ENST00000368428.1:c.12_21del	ENSP00000357413.1:p.Glu5Ter
ENST00000368432.5:c.1098_1107del	ENSP00000357417.1:p.Glu367Ter
ENST00000368433.5:c.*99_*108del	ENSP00000357418.1:n.*99_*108del
ENST00000477609.5:n.70_79del
ENST00000489992.5:n.364+106_364+115del
XM_005245502.2:c.1098_1107del	XP_005245559.1:p.Glu367Ter
XM_005245503.2:c.588_597del	XP_005245560.1:p.Glu197Ter
XR_241098.3:n.1159_1168del