Canonical Allele Identifier: CA1229107887

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240378063C= , CM000663.2:g.240378063C=	GRCh38
NC_000001.10:g.240541363C= , CM000663.1:g.240541363C=	GRCh37
NC_000001.9:g.238607986C=	NCBI36
NG_042054.1:g.291179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14448C= MANE Select	ENSP00000318884.9:n.4859-14448C=
ENST00000545751.3:c.700-14448C=
ENST00000679390.1:n.1121-14448C=
ENST00000679646.1:n.4325-14448C=
ENST00000679980.1:c.1128-14448C=
ENST00000681131.1:c.859-14448C=
ENST00000681210.1:c.1079-14448C=	ENSP00000505131.1:n.1079-14448C=
ENST00000681296.1:n.2046-14448C=
ENST00000681741.1:c.*903-14448C=	ENSP00000505116.1:n.*903-14448C=
ENST00000681805.1:c.744-14448C=
ENST00000681824.1:c.986-14448C=	ENSP00000505818.1:n.986-14448C=
ENST00000319653.13:c.4859-14448C=	ENSP00000318884.9:n.4859-14448C=
ENST00000545751.2:c.287-14448C=	ENSP00000437918.2:n.287-14448C=
NM_001305424.1:c.4871-14448C=	NP_001292353.1:n.4871-14448C=
NM_020066.4:c.4859-14448C=	NP_064450.3:n.4859-14448C=
NM_001348094.1:c.2687-14448C=	NP_001335023.1:n.2687-14448C=
XM_017001840.2:c.2999-14448C=	XP_016857329.1:n.2999-14448C=
XM_017001841.2:c.2999-14448C=	XP_016857330.1:n.2999-14448C=
NM_020066.5:c.4859-14448C= MANE Select	NP_064450.3:n.4859-14448C=
NM_001305424.2:c.4871-14448C=	NP_001292353.1:n.4871-14448C=
NM_001348094.2:c.2687-14448C=	NP_001335023.1:n.2687-14448C=