Canonical Allele Identifier: CA342641314

Gene: FLAD1

Linked Data

• MyVariant Identifiers: chr1:g.154965235T>G (hg19) ; chr1:g.154992759T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992759T>G , CM000663.2:g.154992759T>G	GRCh38
NC_000001.10:g.154965235T>G , CM000663.1:g.154965235T>G	GRCh37
NC_000001.9:g.153231859T>G	NCBI36
NG_042310.1:g.14466T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000292180.8:c.1601T>G MANE Select	ENSP00000292180.3:p.Val534Gly
ENST00000292180.7:c.1601T>G	ENSP00000292180.3:p.Val534Gly
ENST00000295530.6:c.*11+86T>G	ENSP00000295530.2:n.*11+86T>G
ENST00000315144.14:c.1310T>G	ENSP00000317296.10:p.Val437Gly
ENST00000368428.1:c.224T>G	ENSP00000357413.1:p.Val75Gly
ENST00000368432.5:c.1310T>G	ENSP00000357417.1:p.Val437Gly
ENST00000477609.5:n.344+86T>G
ENST00000481758.1:n.171T>G
ENST00000489992.5:n.411T>G
NM_001184891.1:c.1310T>G	NP_001171820.1:p.Val437Gly
NM_025207.4:c.1601T>G	NP_079483.3:p.Val534Gly
NM_201398.2:c.1310T>G	NP_958800.1:p.Val437Gly
XM_005245503.2:c.800T>G	XP_005245560.1:p.Val267Gly
XR_241098.3:n.1371T>G
NM_025207.5:c.1601T>G MANE Select	NP_079483.3:p.Val534Gly
NM_001184891.2:c.1310T>G	NP_001171820.1:p.Val437Gly
NM_201398.3:c.1310T>G	NP_958800.1:p.Val437Gly