Canonical Allele Identifier: CA30901498

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154983727G>C , CM000663.2:g.154983727G>C	GRCh38
NC_000001.10:g.154956203G>C , CM000663.1:g.154956203G>C	GRCh37
NC_000001.9:g.153222827G>C	NCBI36
NG_042310.1:g.5434G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.33G>C MANE Select	ENSP00000292180.3:p.Gln11His
ENST00000292180.7:c.33G>C	ENSP00000292180.3:p.Gln11His
ENST00000315144.14:c.-144-115G>C	ENSP00000317296.10:n.-144-115G>C
ENST00000368431.7:c.-789-115G>C	ENSP00000357416.3:n.-789-115G>C
ENST00000368432.5:c.-144-115G>C	ENSP00000357417.1:n.-144-115G>C
ENST00000368433.5:c.33G>C	ENSP00000357418.1:p.Gln11His
ENST00000487371.1:n.203+94G>C
ENST00000492620.1:n.60+330G>C
NM_001184891.1:c.-144-115G>C	NP_001171820.1:n.-144-115G>C
NM_001184892.1:c.-789-115G>C	NP_001171821.1:n.-789-115G>C
NM_025207.4:c.33G>C	NP_079483.3:p.Gln11His
NM_201398.2:c.-144-115G>C	NP_958800.1:n.-144-115G>C
XM_005245502.2:c.-144-115G>C	XP_005245559.1:n.-144-115G>C
XM_005245503.2:c.-430+330G>C	XP_005245560.1:n.-430+330G>C
XM_006711559.2:c.-144-115G>C	XP_006711622.1:n.-144-115G>C
XR_241098.3:n.66-115G>C
NM_025207.5:c.33G>C MANE Select	NP_079483.3:p.Gln11His
NM_001184891.2:c.-144-115G>C	NP_001171820.1:n.-144-115G>C
NM_001184892.2:c.-789-115G>C	NP_001171821.1:n.-789-115G>C
NM_201398.3:c.-144-115G>C	NP_958800.1:n.-144-115G>C