Canonical Allele Identifier: CA1134300

Gene: FLAD1

Linked Data

• dbSNP Id: rs370022149
• ExAC: 1:154960532 C / T
• gnomAD v2: 1-154960532-C-T
• gnomAD v3: 1-154988056-C-T
• gnomAD v4: 1-154988056-C-T
• MyVariant Identifiers: chr1:g.154960532C>T (hg19) ; chr1:g.154988056C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988056C>T , CM000663.2:g.154988056C>T	GRCh38
NC_000001.10:g.154960532C>T , CM000663.1:g.154960532C>T	GRCh37
NC_000001.9:g.153227156C>T	NCBI36
NG_042310.1:g.9763C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292180.8:c.373-49C>T MANE Select	ENSP00000292180.3:n.373-49C>T
ENST00000292180.7:c.373-49C>T	ENSP00000292180.3:n.373-49C>T
ENST00000315144.14:c.82-49C>T	ENSP00000317296.10:n.82-49C>T
ENST00000368431.7:c.27C>T	ENSP00000357416.3:p.Pro9=
ENST00000368432.5:c.82-49C>T	ENSP00000357417.1:n.82-49C>T
ENST00000368433.5:c.373-49C>T	ENSP00000357418.1:n.373-49C>T
ENST00000487371.1:n.429-49C>T
ENST00000492620.1:n.651C>T
NM_001184891.1:c.82-49C>T	NP_001171820.1:n.82-49C>T
NM_001184892.1:c.27C>T	NP_001171821.1:p.Pro9=
NM_025207.4:c.373-49C>T	NP_079483.3:n.373-49C>T
NM_201398.2:c.82-49C>T	NP_958800.1:n.82-49C>T
XM_005245502.2:c.82-49C>T	XP_005245559.1:n.82-49C>T
XM_005245503.2:c.-429-49C>T	XP_005245560.1:n.-429-49C>T
XM_006711559.2:c.82-49C>T	XP_006711622.1:n.82-49C>T
XR_241098.3:n.291-49C>T
NM_025207.5:c.373-49C>T MANE Select	NP_079483.3:n.373-49C>T
NM_001184891.2:c.82-49C>T	NP_001171820.1:n.82-49C>T
NM_001184892.2:c.27C>T	NP_001171821.1:p.Pro9=
NM_201398.3:c.82-49C>T	NP_958800.1:n.82-49C>T