Canonical Allele Identifier: CA1229067112

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240282416C= , CM000663.2:g.240282416C=	GRCh38
NC_000001.10:g.240445716C= , CM000663.1:g.240445716C=	GRCh37
NC_000001.9:g.238512339C=	NCBI36
NG_042054.1:g.195532C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4154-12406C= MANE Select	ENSP00000318884.9:n.4154-12406C=
ENST00000545751.3:c.57-46660C=
ENST00000679390.1:n.416-12406C=
ENST00000679980.1:c.423-12406C=
ENST00000681131.1:c.81-12406C=
ENST00000681210.1:c.374-12406C=	ENSP00000505131.1:n.374-12406C=
ENST00000681741.1:c.*198-12406C=	ENSP00000505116.1:n.*198-12406C=
ENST00000681805.1:c.39-12406C=
ENST00000681824.1:c.374-12406C=	ENSP00000505818.1:n.374-12406C=
ENST00000319653.13:c.4154-12406C=	ENSP00000318884.9:n.4154-12406C=
ENST00000441342.1:c.92-12406C=	ENSP00000388922.1:n.92-12406C=
ENST00000463398.5:n.214-12406C=
NM_001305424.1:c.4166-12406C=	NP_001292353.1:n.4166-12406C=
NM_020066.4:c.4154-12406C=	NP_064450.3:n.4154-12406C=
NM_001348094.1:c.2075-12406C=	NP_001335023.1:n.2075-12406C=
XM_017001837.1:c.4166-12406C=	XP_016857326.1:n.4166-12406C=
XM_017001840.2:c.2294-12406C=	XP_016857329.1:n.2294-12406C=
XM_017001841.2:c.2294-12406C=	XP_016857330.1:n.2294-12406C=
NM_020066.5:c.4154-12406C= MANE Select	NP_064450.3:n.4154-12406C=
NM_001305424.2:c.4166-12406C=	NP_001292353.1:n.4166-12406C=
NM_001348094.2:c.2075-12406C=	NP_001335023.1:n.2075-12406C=