Canonical Allele Identifier: CA30905385

Gene: FLAD1

Linked Data

• ClinVar Variation Id: 1956525
• ClinVar RCV Id: RCV002720277
• dbSNP Id: rs920886455
• gnomAD v3: 1-154988264-G-A
• gnomAD v4: 1-154988264-G-A
• MyVariant Identifiers: chr1:g.154960740G>A (hg19) ; chr1:g.154988264G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988264G>A , CM000663.2:g.154988264G>A	GRCh38
NC_000001.10:g.154960740G>A , CM000663.1:g.154960740G>A	GRCh37
NC_000001.9:g.153227364G>A	NCBI36
NG_042310.1:g.9971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.532G>A MANE Select	ENSP00000292180.3:p.Gly178Ser
ENST00000292180.7:c.532G>A	ENSP00000292180.3:p.Gly178Ser
ENST00000295530.6:c.-270G>A	ENSP00000295530.2:n.-270G>A
ENST00000315144.14:c.241G>A	ENSP00000317296.10:p.Gly81Ser
ENST00000368431.7:c.235G>A	ENSP00000357416.3:p.Gly79Ser
ENST00000368432.5:c.241G>A	ENSP00000357417.1:p.Gly81Ser
ENST00000368433.5:c.532G>A	ENSP00000357418.1:p.Gly178Ser
ENST00000487371.1:n.588G>A
NM_001184891.1:c.241G>A	NP_001171820.1:p.Gly81Ser
NM_001184892.1:c.235G>A	NP_001171821.1:p.Gly79Ser
NM_025207.4:c.532G>A	NP_079483.3:p.Gly178Ser
NM_201398.2:c.241G>A	NP_958800.1:p.Gly81Ser
XM_005245502.2:c.241G>A	XP_005245559.1:p.Gly81Ser
XM_005245503.2:c.-270G>A	XP_005245560.1:n.-270G>A
XM_006711559.2:c.241G>A	XP_006711622.1:p.Gly81Ser
XR_241098.3:n.450G>A
NM_025207.5:c.532G>A MANE Select	NP_079483.3:p.Gly178Ser
NM_001184891.2:c.241G>A	NP_001171820.1:p.Gly81Ser
NM_001184892.2:c.235G>A	NP_001171821.1:p.Gly79Ser
NM_201398.3:c.241G>A	NP_958800.1:p.Gly81Ser