Canonical Allele Identifier: CA2838227700

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32989230T>C , CM000677.2:g.32989230T>C	GRCh38
NC_000015.9:g.33281431T>C , CM000677.1:g.33281431T>C	GRCh37
NC_000015.8:g.31068723T>C	NCBI36
NG_042863.1:g.210504A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616417.5:c.2223+18784A>G MANE Select	ENSP00000479134.1:n.2223+18784A>G
ENST00000672206.1:c.489+18784A>G	ENSP00000500647.1:n.489+18784A>G
ENST00000334528.13:c.1554+18784A>G	ENSP00000333950.9:n.1554+18784A>G
ENST00000559047.5:c.2223+18784A>G	ENSP00000454047.1:n.2223+18784A>G
ENST00000561249.5:c.1929+18784A>G	ENSP00000453443.1:n.1929+18784A>G
ENST00000616417.4:c.2223+18784A>G	ENSP00000479134.1:n.2223+18784A>G
NM_001103184.3:c.1554+18784A>G	NP_001096654.1:n.1554+18784A>G
NM_001277313.1:c.2223+18784A>G	NP_001264242.1:n.2223+18784A>G
XM_011521504.1:c.2223+18784A>G	XP_011519806.1:n.2223+18784A>G
XM_011521505.1:c.2223+18784A>G	XP_011519807.1:n.2223+18784A>G
XM_011521506.1:c.1929+18784A>G	XP_011519808.1:n.1929+18784A>G
XM_011521507.1:c.2223+18784A>G	XP_011519809.1:n.2223+18784A>G
XM_011521508.1:c.2223+18784A>G	XP_011519810.1:n.2223+18784A>G
XM_011521509.1:c.573+18784A>G	XP_011519811.1:n.573+18784A>G
XM_011521510.1:c.480+18784A>G	XP_011519812.1:n.480+18784A>G
XM_011521511.1:c.447+18784A>G	XP_011519813.1:n.447+18784A>G
XM_011521504.3:c.2223+18784A>G	XP_011519806.1:n.2223+18784A>G
XM_011521505.2:c.2223+18784A>G	XP_011519807.1:n.2223+18784A>G
XM_011521506.3:c.1929+18784A>G	XP_011519808.1:n.1929+18784A>G
XM_011521507.2:c.2223+18784A>G	XP_011519809.1:n.2223+18784A>G
XM_011521509.3:c.573+18784A>G	XP_011519811.1:n.573+18784A>G
XM_011521511.3:c.447+18784A>G	XP_011519813.1:n.447+18784A>G
XM_017022130.2:c.2223+18784A>G	XP_016877619.1:n.2223+18784A>G
XM_017022131.1:c.2223+18784A>G	XP_016877620.1:n.2223+18784A>G
XM_017022132.2:c.489+18784A>G	XP_016877621.1:n.489+18784A>G
XM_017022133.2:c.393+18784A>G	XP_016877622.1:n.393+18784A>G
XM_017022134.2:c.390+18784A>G	XP_016877623.1:n.390+18784A>G
XM_017022135.2:c.214-19753A>G	XP_016877624.1:n.214-19753A>G
NM_001103184.4:c.1554+18784A>G	NP_001096654.1:n.1554+18784A>G
NM_001277313.2:c.2223+18784A>G MANE Select	NP_001264242.1:n.2223+18784A>G