Canonical Allele Identifier: CA342742211

Gene: FLAD1

Linked Data

• MyVariant Identifiers: chr1:g.154960623C>A (hg19) ; chr1:g.154988147C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988147C>A , CM000663.2:g.154988147C>A	GRCh38
NC_000001.10:g.154960623C>A , CM000663.1:g.154960623C>A	GRCh37
NC_000001.9:g.153227247C>A	NCBI36
NG_042310.1:g.9854C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292180.8:c.415C>A MANE Select	ENSP00000292180.3:p.Leu139Met
ENST00000292180.7:c.415C>A	ENSP00000292180.3:p.Leu139Met
ENST00000295530.6:c.-387C>A	ENSP00000295530.2:n.-387C>A
ENST00000315144.14:c.124C>A	ENSP00000317296.10:p.Leu42Met
ENST00000368431.7:c.118C>A	ENSP00000357416.3:p.Leu40Met
ENST00000368432.5:c.124C>A	ENSP00000357417.1:p.Leu42Met
ENST00000368433.5:c.415C>A	ENSP00000357418.1:p.Leu139Met
ENST00000487371.1:n.471C>A
NM_001184891.1:c.124C>A	NP_001171820.1:p.Leu42Met
NM_001184892.1:c.118C>A	NP_001171821.1:p.Leu40Met
NM_025207.4:c.415C>A	NP_079483.3:p.Leu139Met
NM_201398.2:c.124C>A	NP_958800.1:p.Leu42Met
XM_005245502.2:c.124C>A	XP_005245559.1:p.Leu42Met
XM_005245503.2:c.-387C>A	XP_005245560.1:n.-387C>A
XM_006711559.2:c.124C>A	XP_006711622.1:p.Leu42Met
XR_241098.3:n.333C>A
NM_025207.5:c.415C>A MANE Select	NP_079483.3:p.Leu139Met
NM_001184891.2:c.124C>A	NP_001171820.1:p.Leu42Met
NM_001184892.2:c.118C>A	NP_001171821.1:p.Leu40Met
NM_201398.3:c.124C>A	NP_958800.1:p.Leu42Met