Canonical Allele Identifier: CA1134360

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988341C>T , CM000663.2:g.154988341C>T	GRCh38
NC_000001.10:g.154960817C>T , CM000663.1:g.154960817C>T	GRCh37
NC_000001.9:g.153227441C>T	NCBI36
NG_042310.1:g.10048C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.609C>T MANE Select	ENSP00000292180.3:p.Pro203=
ENST00000292180.7:c.609C>T	ENSP00000292180.3:p.Pro203=
ENST00000295530.6:c.-193C>T	ENSP00000295530.2:n.-193C>T
ENST00000315144.14:c.318C>T	ENSP00000317296.10:p.Pro106=
ENST00000368431.7:c.312C>T	ENSP00000357416.3:p.Pro104=
ENST00000368432.5:c.318C>T	ENSP00000357417.1:p.Pro106=
ENST00000368433.5:c.609C>T	ENSP00000357418.1:p.Pro203=
ENST00000487371.1:n.665C>T
NM_001184891.1:c.318C>T	NP_001171820.1:p.Pro106=
NM_001184892.1:c.312C>T	NP_001171821.1:p.Pro104=
NM_025207.4:c.609C>T	NP_079483.3:p.Pro203=
NM_201398.2:c.318C>T	NP_958800.1:p.Pro106=
XM_005245502.2:c.318C>T	XP_005245559.1:p.Pro106=
XM_005245503.2:c.-193C>T	XP_005245560.1:n.-193C>T
XM_006711559.2:c.318C>T	XP_006711622.1:p.Pro106=
XR_241098.3:n.527C>T
NM_025207.5:c.609C>T MANE Select	NP_079483.3:p.Pro203=
NM_001184891.2:c.318C>T	NP_001171820.1:p.Pro106=
NM_001184892.2:c.312C>T	NP_001171821.1:p.Pro104=
NM_201398.3:c.318C>T	NP_958800.1:p.Pro106=