Canonical Allele Identifier: CA1134240

Gene: FLAD1

Linked Data

• dbSNP Id: rs781322149
• ExAC: 1:154956328 C / G
• gnomAD v2: 1-154956328-C-G
• MyVariant Identifiers: chr1:g.154956328C>G (hg19) ; chr1:g.154983852C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154983852C>G , CM000663.2:g.154983852C>G	GRCh38
NC_000001.10:g.154956328C>G , CM000663.1:g.154956328C>G	GRCh37
NC_000001.9:g.153222952C>G	NCBI36
NG_042310.1:g.5559C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.158C>G MANE Select	ENSP00000292180.3:p.Thr53Ser
ENST00000292180.7:c.158C>G	ENSP00000292180.3:p.Thr53Ser
ENST00000315144.14:c.-134C>G	ENSP00000317296.10:n.-134C>G
ENST00000368431.7:c.-779C>G	ENSP00000357416.3:n.-779C>G
ENST00000368432.5:c.-134C>G	ENSP00000357417.1:n.-134C>G
ENST00000368433.5:c.158C>G	ENSP00000357418.1:p.Thr53Ser
ENST00000487371.1:n.214C>G
ENST00000492620.1:n.60+455C>G
NM_001184891.1:c.-134C>G	NP_001171820.1:n.-134C>G
NM_001184892.1:c.-779C>G	NP_001171821.1:n.-779C>G
NM_025207.4:c.158C>G	NP_079483.3:p.Thr53Ser
NM_201398.2:c.-134C>G	NP_958800.1:n.-134C>G
XM_005245502.2:c.-134C>G	XP_005245559.1:n.-134C>G
XM_005245503.2:c.-430+455C>G	XP_005245560.1:n.-430+455C>G
XM_006711559.2:c.-134C>G	XP_006711622.1:n.-134C>G
XR_241098.3:n.76C>G
NM_025207.5:c.158C>G MANE Select	NP_079483.3:p.Thr53Ser
NM_001184891.2:c.-134C>G	NP_001171820.1:n.-134C>G
NM_001184892.2:c.-779C>G	NP_001171821.1:n.-779C>G
NM_201398.3:c.-134C>G	NP_958800.1:n.-134C>G