Canonical Allele Identifier: CA1134626

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992724C>T , CM000663.2:g.154992724C>T	GRCh38
NC_000001.10:g.154965200C>T , CM000663.1:g.154965200C>T	GRCh37
NC_000001.9:g.153231824C>T	NCBI36
NG_042310.1:g.14431C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.1566C>T MANE Select	ENSP00000292180.3:p.Tyr522=
ENST00000292180.7:c.1566C>T	ENSP00000292180.3:p.Tyr522=
ENST00000295530.6:c.*11+51C>T	ENSP00000295530.2:n.*11+51C>T
ENST00000315144.14:c.1275C>T	ENSP00000317296.10:p.Tyr425=
ENST00000368428.1:c.189C>T	ENSP00000357413.1:p.Tyr63=
ENST00000368432.5:c.1275C>T	ENSP00000357417.1:p.Tyr425=
ENST00000477609.5:n.344+51C>T
ENST00000481758.1:n.136C>T
ENST00000489992.5:n.376C>T
NM_001184891.1:c.1275C>T	NP_001171820.1:p.Tyr425=
NM_025207.4:c.1566C>T	NP_079483.3:p.Tyr522=
NM_201398.2:c.1275C>T	NP_958800.1:p.Tyr425=
XM_005245503.2:c.765C>T	XP_005245560.1:p.Tyr255=
XR_241098.3:n.1336C>T
NM_025207.5:c.1566C>T MANE Select	NP_079483.3:p.Tyr522=
NM_001184891.2:c.1275C>T	NP_001171820.1:p.Tyr425=
NM_201398.3:c.1275C>T	NP_958800.1:p.Tyr425=