Canonical Allele Identifier: CA15848008
Gene: FMN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.32964050T>C , CM000677.2:g.32964050T>C GRCh38
NC_000015.9:g.33256251T>C , CM000677.1:g.33256251T>C GRCh37
NC_000015.8:g.31043543T>C NCBI36
NG_042863.1:g.235684A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001277313.2:c.3138+57A>G MANE Select NP_001264242.1:n.3138+57A>G
ENST00000616417.5:c.3138+57A>G MANE Select ENSP00000479134.1:n.3138+57A>G
NM_001103184.3:c.2469+57A>G NP_001096654.1:n.2469+57A>G
NM_001103184.4:c.2469+57A>G NP_001096654.1:n.2469+57A>G
NM_001277313.1:c.3138+57A>G NP_001264242.1:n.3138+57A>G
ENST00000334528.13:c.2469+57A>G ENSP00000333950.9:n.2469+57A>G
ENST00000559047.5:c.3138+57A>G ENSP00000454047.1:n.3138+57A>G
ENST00000561249.5:c.2844+57A>G ENSP00000453443.1:n.2844+57A>G
ENST00000616417.4:c.3138+57A>G ENSP00000479134.1:n.3138+57A>G
ENST00000672206.1:c.1404+57A>G ENSP00000500647.1:n.1404+57A>G
XM_011521504.1:c.3138+57A>G XP_011519806.1:n.3138+57A>G
XM_011521504.3:c.3138+57A>G XP_011519806.1:n.3138+57A>G
XM_011521505.1:c.3138+57A>G XP_011519807.1:n.3138+57A>G
XM_011521505.2:c.3138+57A>G XP_011519807.1:n.3138+57A>G
XM_011521506.1:c.2844+57A>G XP_011519808.1:n.2844+57A>G
XM_011521506.3:c.2844+57A>G XP_011519808.1:n.2844+57A>G
XM_011521507.1:c.3138+57A>G XP_011519809.1:n.3138+57A>G
XM_011521507.2:c.3138+57A>G XP_011519809.1:n.3138+57A>G
XM_011521508.1:c.3138+57A>G XP_011519810.1:n.3138+57A>G
XM_011521509.1:c.1488+57A>G XP_011519811.1:n.1488+57A>G
XM_011521509.3:c.1488+57A>G XP_011519811.1:n.1488+57A>G
XM_011521510.1:c.1395+57A>G XP_011519812.1:n.1395+57A>G
XM_011521511.1:c.1362+57A>G XP_011519813.1:n.1362+57A>G
XM_011521511.3:c.1362+57A>G XP_011519813.1:n.1362+57A>G
XM_011521512.1:c.948+57A>G XP_011519814.1:n.948+57A>G
XM_017022130.2:c.3138+57A>G XP_016877619.1:n.3138+57A>G
XM_017022131.1:c.3138+57A>G XP_016877620.1:n.3138+57A>G
XM_017022132.2:c.1404+57A>G XP_016877621.1:n.1404+57A>G
XM_017022133.2:c.1308+57A>G XP_016877622.1:n.1308+57A>G
XM_017022134.2:c.1305+57A>G XP_016877623.1:n.1305+57A>G
XM_017022135.2:c.1128+57A>G XP_016877624.1:n.1128+57A>G