Canonical Allele Identifier: CA268489726

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32776689_32776690insCT , CM000677.2:g.32776689_32776690insCT	GRCh38
NC_000015.9:g.33068890_33068891insCT , CM000677.1:g.33068890_33068891insCT	GRCh37
NC_000015.8:g.30856182_30856183insCT	NCBI36
NG_042863.1:g.423045_423046insGA

Transcript Alleles

HGVS	Amino-acid Change
NM_001277313.2:c.4215+146_4215+147insGA MANE Select	NP_001264242.1:n.4215+146_4215+147insGA
ENST00000616417.5:c.4215+146_4215+147insGA MANE Select	ENSP00000479134.1:n.4215+146_4215+147insGA
NM_001103184.3:c.3546+146_3546+147insGA	NP_001096654.1:n.3546+146_3546+147insGA
NM_001103184.4:c.3546+146_3546+147insGA	NP_001096654.1:n.3546+146_3546+147insGA
NM_001277313.1:c.4215+146_4215+147insGA	NP_001264242.1:n.4215+146_4215+147insGA
ENST00000334528.13:c.3546+146_3546+147insGA	ENSP00000333950.9:n.3546+146_3546+147insGA
ENST00000558882.1:n.538+146_538+147insGA
ENST00000559047.5:c.4215+146_4215+147insGA	ENSP00000454047.1:n.4215+146_4215+147insGA
ENST00000561249.5:c.3921+146_3921+147insGA	ENSP00000453443.1:n.3921+146_3921+147insGA
ENST00000616417.4:c.4215+146_4215+147insGA	ENSP00000479134.1:n.4215+146_4215+147insGA
ENST00000672206.1:c.2481+146_2481+147insGA	ENSP00000500647.1:n.2481+146_2481+147insGA
XM_011521504.1:c.4215+146_4215+147insGA	XP_011519806.1:n.4215+146_4215+147insGA
XM_011521504.3:c.4215+146_4215+147insGA	XP_011519806.1:n.4215+146_4215+147insGA
XM_011521506.1:c.3921+146_3921+147insGA	XP_011519808.1:n.3921+146_3921+147insGA
XM_011521506.3:c.3921+146_3921+147insGA	XP_011519808.1:n.3921+146_3921+147insGA
XM_011521509.1:c.2565+146_2565+147insGA	XP_011519811.1:n.2565+146_2565+147insGA
XM_011521509.3:c.2565+146_2565+147insGA	XP_011519811.1:n.2565+146_2565+147insGA
XM_011521510.1:c.2472+146_2472+147insGA	XP_011519812.1:n.2472+146_2472+147insGA
XM_011521511.1:c.2439+146_2439+147insGA	XP_011519813.1:n.2439+146_2439+147insGA
XM_011521511.3:c.2439+146_2439+147insGA	XP_011519813.1:n.2439+146_2439+147insGA
XM_011521512.1:c.2025+146_2025+147insGA	XP_011519814.1:n.2025+146_2025+147insGA
XM_017022130.2:c.4215+146_4215+147insGA	XP_016877619.1:n.4215+146_4215+147insGA
XM_017022132.2:c.2481+146_2481+147insGA	XP_016877621.1:n.2481+146_2481+147insGA
XM_017022133.2:c.2385+146_2385+147insGA	XP_016877622.1:n.2385+146_2385+147insGA
XM_017022134.2:c.2382+146_2382+147insGA	XP_016877623.1:n.2382+146_2382+147insGA
XM_017022135.2:c.2205+146_2205+147insGA	XP_016877624.1:n.2205+146_2205+147insGA