Canonical Allele Identifier: CA1134484
Community Standard Title: NM_025207.5(FLAD1):c.1118-33C>T
Gene: FLAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154989527C>T , CM000663.2:g.154989527C>T GRCh38
NC_000001.10:g.154962003C>T , CM000663.1:g.154962003C>T GRCh37
NC_000001.9:g.153228627C>T NCBI36
NG_042310.1:g.11234C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025207.5:c.1118-33C>T MANE Select NP_079483.3:n.1118-33C>T
ENST00000292180.8:c.1118-33C>T MANE Select ENSP00000292180.3:n.1118-33C>T
NM_001184891.1:c.827-33C>T NP_001171820.1:n.827-33C>T
NM_001184891.2:c.827-33C>T NP_001171820.1:n.827-33C>T
NM_025207.4:c.1118-33C>T NP_079483.3:n.1118-33C>T
NM_201398.2:c.827-33C>T NP_958800.1:n.827-33C>T
NM_201398.3:c.827-33C>T NP_958800.1:n.827-33C>T
ENST00000292180.7:c.1118-33C>T ENSP00000292180.3:n.1118-33C>T
ENST00000295530.6:c.317-632C>T ENSP00000295530.2:n.317-632C>T
ENST00000315144.14:c.827-33C>T ENSP00000317296.10:n.827-33C>T
ENST00000368428.1:c.-341-33C>T ENSP00000357413.1:n.-341-33C>T
ENST00000368432.5:c.827-33C>T ENSP00000357417.1:n.827-33C>T
ENST00000368433.5:c.1118-33C>T ENSP00000357418.1:n.1118-33C>T
ENST00000489992.5:n.266-632C>T
XM_005245502.2:c.827-33C>T XP_005245559.1:n.827-33C>T
XM_005245503.2:c.317-33C>T XP_005245560.1:n.317-33C>T
XM_006711559.2:c.827-53C>T XP_006711622.1:n.827-53C>T
XR_241098.3:n.1036-632C>T