Canonical Allele Identifier: CA7457477

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.33088784A>C , CM000677.2:g.33088784A>C	GRCh38
NC_000015.9:g.33380985A>C , CM000677.1:g.33380985A>C	GRCh37
NC_000015.8:g.31168277A>C	NCBI36
NG_042863.1:g.110950T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001277313.2:c.2043+15T>G MANE Select	NP_001264242.1:n.2043+15T>G
ENST00000616417.5:c.2043+15T>G MANE Select	ENSP00000479134.1:n.2043+15T>G
NM_001277313.1:c.2043+15T>G	NP_001264242.1:n.2043+15T>G
ENST00000559047.5:c.2043+15T>G	ENSP00000454047.1:n.2043+15T>G
ENST00000561249.5:c.1867+64264T>G	ENSP00000453443.1:n.1867+64264T>G
ENST00000616417.4:c.2043+15T>G	ENSP00000479134.1:n.2043+15T>G
ENST00000672206.1:c.309+15T>G	ENSP00000500647.1:n.309+15T>G
ENST00000674090.1:n.416+15T>G
XM_011521504.1:c.2043+15T>G	XP_011519806.1:n.2043+15T>G
XM_011521504.3:c.2043+15T>G	XP_011519806.1:n.2043+15T>G
XM_011521505.1:c.2043+15T>G	XP_011519807.1:n.2043+15T>G
XM_011521505.2:c.2043+15T>G	XP_011519807.1:n.2043+15T>G
XM_011521506.1:c.1867+64264T>G	XP_011519808.1:n.1867+64264T>G
XM_011521506.3:c.1867+64264T>G	XP_011519808.1:n.1867+64264T>G
XM_011521507.1:c.2043+15T>G	XP_011519809.1:n.2043+15T>G
XM_011521507.2:c.2043+15T>G	XP_011519809.1:n.2043+15T>G
XM_011521508.1:c.2043+15T>G	XP_011519810.1:n.2043+15T>G
XM_011521509.1:c.393+15T>G	XP_011519811.1:n.393+15T>G
XM_011521509.3:c.393+15T>G	XP_011519811.1:n.393+15T>G
XM_011521510.1:c.300+15T>G	XP_011519812.1:n.300+15T>G
XM_011521511.1:c.267+15T>G	XP_011519813.1:n.267+15T>G
XM_011521511.3:c.267+15T>G	XP_011519813.1:n.267+15T>G
XM_017022130.2:c.2043+15T>G	XP_016877619.1:n.2043+15T>G
XM_017022131.1:c.2043+15T>G	XP_016877620.1:n.2043+15T>G
XM_017022132.2:c.309+15T>G	XP_016877621.1:n.309+15T>G
XM_017022133.2:c.214-23710T>G	XP_016877622.1:n.214-23710T>G
XM_017022134.2:c.210+15T>G	XP_016877623.1:n.210+15T>G
XM_017022135.2:c.213+64264T>G	XP_016877624.1:n.213+64264T>G