Canonical Allele Identifier: CA14200263

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32888031A>G , CM000677.2:g.32888031A>G	GRCh38
NC_000015.9:g.33180232A>G , CM000677.1:g.33180232A>G	GRCh37
NC_000015.8:g.30967524A>G	NCBI36
NG_042863.1:g.311703T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616417.5:c.3835+141T>C MANE Select	ENSP00000479134.1:n.3835+141T>C
ENST00000672206.1:c.2101+141T>C	ENSP00000500647.1:n.2101+141T>C
ENST00000334528.13:c.3166+141T>C	ENSP00000333950.9:n.3166+141T>C
ENST00000559047.5:c.3835+141T>C	ENSP00000454047.1:n.3835+141T>C
ENST00000559610.1:c.83+141T>C
ENST00000561249.5:c.3541+141T>C	ENSP00000453443.1:n.3541+141T>C
ENST00000616417.4:c.3835+141T>C	ENSP00000479134.1:n.3835+141T>C
NM_001103184.3:c.3166+141T>C	NP_001096654.1:n.3166+141T>C
NM_001277313.1:c.3835+141T>C	NP_001264242.1:n.3835+141T>C
XM_011521504.1:c.3835+141T>C	XP_011519806.1:n.3835+141T>C
XM_011521505.1:c.3835+141T>C	XP_011519807.1:n.3835+141T>C
XM_011521506.1:c.3541+141T>C	XP_011519808.1:n.3541+141T>C
XM_011521507.1:c.3835+141T>C	XP_011519809.1:n.3835+141T>C
XM_011521509.1:c.2185+141T>C	XP_011519811.1:n.2185+141T>C
XM_011521510.1:c.2092+141T>C	XP_011519812.1:n.2092+141T>C
XM_011521511.1:c.2059+141T>C	XP_011519813.1:n.2059+141T>C
XM_011521512.1:c.1645+141T>C	XP_011519814.1:n.1645+141T>C
XM_011521504.3:c.3835+141T>C	XP_011519806.1:n.3835+141T>C
XM_011521505.2:c.3835+141T>C	XP_011519807.1:n.3835+141T>C
XM_011521506.3:c.3541+141T>C	XP_011519808.1:n.3541+141T>C
XM_011521507.2:c.3835+141T>C	XP_011519809.1:n.3835+141T>C
XM_011521509.3:c.2185+141T>C	XP_011519811.1:n.2185+141T>C
XM_011521511.3:c.2059+141T>C	XP_011519813.1:n.2059+141T>C
XM_017022130.2:c.3835+141T>C	XP_016877619.1:n.3835+141T>C
XM_017022131.1:c.3835+141T>C	XP_016877620.1:n.3835+141T>C
XM_017022132.2:c.2101+141T>C	XP_016877621.1:n.2101+141T>C
XM_017022133.2:c.2005+141T>C	XP_016877622.1:n.2005+141T>C
XM_017022134.2:c.2002+141T>C	XP_016877623.1:n.2002+141T>C
XM_017022135.2:c.1825+141T>C	XP_016877624.1:n.1825+141T>C
NM_001103184.4:c.3166+141T>C	NP_001096654.1:n.3166+141T>C
NM_001277313.2:c.3835+141T>C MANE Select	NP_001264242.1:n.3835+141T>C