Canonical Allele Identifier: CA14115899

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32798683T>G , CM000677.2:g.32798683T>G	GRCh38
NC_000015.9:g.33090884T>G , CM000677.1:g.33090884T>G	GRCh37
NC_000015.8:g.30878176T>G	NCBI36
NG_042863.1:g.401051A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001277313.2:c.4130+121A>C MANE Select	NP_001264242.1:n.4130+121A>C
ENST00000616417.5:c.4130+121A>C MANE Select	ENSP00000479134.1:n.4130+121A>C
NM_001103184.3:c.3461+121A>C	NP_001096654.1:n.3461+121A>C
NM_001103184.4:c.3461+121A>C	NP_001096654.1:n.3461+121A>C
NM_001277313.1:c.4130+121A>C	NP_001264242.1:n.4130+121A>C
ENST00000334528.13:c.3461+121A>C	ENSP00000333950.9:n.3461+121A>C
ENST00000558882.1:n.453+121A>C
ENST00000559047.5:c.4130+121A>C	ENSP00000454047.1:n.4130+121A>C
ENST00000561249.5:c.3836+121A>C	ENSP00000453443.1:n.3836+121A>C
ENST00000616417.4:c.4130+121A>C	ENSP00000479134.1:n.4130+121A>C
ENST00000672206.1:c.2396+121A>C	ENSP00000500647.1:n.2396+121A>C
XM_011521504.1:c.4130+121A>C	XP_011519806.1:n.4130+121A>C
XM_011521504.3:c.4130+121A>C	XP_011519806.1:n.4130+121A>C
XM_011521506.1:c.3836+121A>C	XP_011519808.1:n.3836+121A>C
XM_011521506.3:c.3836+121A>C	XP_011519808.1:n.3836+121A>C
XM_011521509.1:c.2480+121A>C	XP_011519811.1:n.2480+121A>C
XM_011521509.3:c.2480+121A>C	XP_011519811.1:n.2480+121A>C
XM_011521510.1:c.2387+121A>C	XP_011519812.1:n.2387+121A>C
XM_011521511.1:c.2354+121A>C	XP_011519813.1:n.2354+121A>C
XM_011521511.3:c.2354+121A>C	XP_011519813.1:n.2354+121A>C
XM_011521512.1:c.1940+121A>C	XP_011519814.1:n.1940+121A>C
XM_017022130.2:c.4130+121A>C	XP_016877619.1:n.4130+121A>C
XM_017022132.2:c.2396+121A>C	XP_016877621.1:n.2396+121A>C
XM_017022133.2:c.2300+121A>C	XP_016877622.1:n.2300+121A>C
XM_017022134.2:c.2297+121A>C	XP_016877623.1:n.2297+121A>C
XM_017022135.2:c.2120+121A>C	XP_016877624.1:n.2120+121A>C
XR_002957769.1:n.297-12235T>G
XR_002957770.1:n.297-12235T>G