Canonical Allele Identifier: CA7457245

Gene: FMN1

Linked Data

• ClinVar Variation Id: 499460
• ClinVar RCV Id: RCV000598374 ; RCV004024765
• dbSNP Id: rs201609721
• ExAC: 15:33359199 G / A
• gnomAD v2: 15-33359199-G-A
• gnomAD v3: 15-33066998-G-A
• gnomAD v4: 15-33066998-G-A
• MyVariant Identifiers: chr15:g.33359199G>A (hg19) ; chr15:g.33066998G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.33066998G>A , CM000677.2:g.33066998G>A	GRCh38
NC_000015.9:g.33359199G>A , CM000677.1:g.33359199G>A	GRCh37
NC_000015.8:g.31146491G>A	NCBI36
NG_042863.1:g.132736C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616417.5:c.2044-1924C>T MANE Select	ENSP00000479134.1:n.2044-1924C>T
ENST00000672206.1:c.310-1924C>T	ENSP00000500647.1:n.310-1924C>T
ENST00000674090.1:n.417-1924C>T
ENST00000334528.13:c.887C>T	ENSP00000333950.9:p.Thr296Met
ENST00000558197.1:c.887C>T	ENSP00000452984.1:p.Thr296Met
ENST00000559047.5:c.2044-1924C>T	ENSP00000454047.1:n.2044-1924C>T
ENST00000559150.1:n.239+796C>T
ENST00000561249.5:c.1868-58923C>T	ENSP00000453443.1:n.1868-58923C>T
ENST00000616417.4:c.2044-1924C>T	ENSP00000479134.1:n.2044-1924C>T
NM_001103184.3:c.887C>T	NP_001096654.1:p.Thr296Met
NM_001277313.1:c.2044-1924C>T	NP_001264242.1:n.2044-1924C>T
XM_011521504.1:c.2044-1924C>T	XP_011519806.1:n.2044-1924C>T
XM_011521505.1:c.2044-1924C>T	XP_011519807.1:n.2044-1924C>T
XM_011521506.1:c.1868-58923C>T	XP_011519808.1:n.1868-58923C>T
XM_011521507.1:c.2044-1924C>T	XP_011519809.1:n.2044-1924C>T
XM_011521508.1:c.2044-1924C>T	XP_011519810.1:n.2044-1924C>T
XM_011521509.1:c.394-1924C>T	XP_011519811.1:n.394-1924C>T
XM_011521510.1:c.301-1924C>T	XP_011519812.1:n.301-1924C>T
XM_011521511.1:c.268-1924C>T	XP_011519813.1:n.268-1924C>T
XM_011521504.3:c.2044-1924C>T	XP_011519806.1:n.2044-1924C>T
XM_011521505.2:c.2044-1924C>T	XP_011519807.1:n.2044-1924C>T
XM_011521506.3:c.1868-58923C>T	XP_011519808.1:n.1868-58923C>T
XM_011521507.2:c.2044-1924C>T	XP_011519809.1:n.2044-1924C>T
XM_011521509.3:c.394-1924C>T	XP_011519811.1:n.394-1924C>T
XM_011521511.3:c.268-1924C>T	XP_011519813.1:n.268-1924C>T
XM_017022130.2:c.2044-1924C>T	XP_016877619.1:n.2044-1924C>T
XM_017022131.1:c.2044-1924C>T	XP_016877620.1:n.2044-1924C>T
XM_017022132.2:c.310-1924C>T	XP_016877621.1:n.310-1924C>T
XM_017022133.2:c.214-1924C>T	XP_016877622.1:n.214-1924C>T
XM_017022134.2:c.211-1924C>T	XP_016877623.1:n.211-1924C>T
XM_017022135.2:c.213+86050C>T	XP_016877624.1:n.213+86050C>T
NM_001103184.4:c.887C>T	NP_001096654.1:p.Thr296Met
NM_001277313.2:c.2044-1924C>T MANE Select	NP_001264242.1:n.2044-1924C>T