Canonical Allele Identifier: CA7457608

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.33154678G>T , CM000677.2:g.33154678G>T	GRCh38
NC_000015.9:g.33446879G>T , CM000677.1:g.33446879G>T	GRCh37
NC_000015.8:g.31234171G>T	NCBI36
NG_042863.1:g.45056C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616417.5:c.237C>A MANE Select	ENSP00000479134.1:p.Pro79=
ENST00000674090.1:n.169+25520C>A
ENST00000320930.7:c.237C>A	ENSP00000325166.7:p.Pro79=
ENST00000559047.5:c.237C>A	ENSP00000454047.1:p.Pro79=
ENST00000561249.5:c.237C>A	ENSP00000453443.1:p.Pro79=
ENST00000616417.4:c.237C>A	ENSP00000479134.1:p.Pro79=
NM_001277313.1:c.237C>A	NP_001264242.1:p.Pro79=
NM_001277314.1:c.237C>A	NP_001264243.1:p.Pro79=
XM_011521504.1:c.237C>A	XP_011519806.1:p.Pro79=
XM_011521505.1:c.237C>A	XP_011519807.1:p.Pro79=
XM_011521506.1:c.237C>A	XP_011519808.1:p.Pro79=
XM_011521507.1:c.237C>A	XP_011519809.1:p.Pro79=
XM_011521508.1:c.237C>A	XP_011519810.1:p.Pro79=
XM_011521509.1:c.217+25520C>A	XP_011519811.1:n.217+25520C>A
XM_011521504.3:c.237C>A	XP_011519806.1:p.Pro79=
XM_011521505.2:c.237C>A	XP_011519807.1:p.Pro79=
XM_011521506.3:c.237C>A	XP_011519808.1:p.Pro79=
XM_011521507.2:c.237C>A	XP_011519809.1:p.Pro79=
XM_011521509.3:c.217+25520C>A	XP_011519811.1:n.217+25520C>A
XM_017022130.2:c.237C>A	XP_016877619.1:p.Pro79=
XM_017022131.1:c.237C>A	XP_016877620.1:p.Pro79=
XM_017022133.2:c.-1418C>A	XP_016877622.1:n.-1418C>A
XM_017022135.2:c.-1418C>A	XP_016877624.1:n.-1418C>A
NM_001277313.2:c.237C>A MANE Select	NP_001264242.1:p.Pro79=
NM_001277314.2:c.237C>A	NP_001264243.1:p.Pro79=