Canonical Allele Identifier: CA1228998364

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240123320C= , CM000663.2:g.240123320C=	GRCh38
NC_000001.10:g.240286620C= , CM000663.1:g.240286620C=	GRCh37
NC_000001.9:g.238353243C=	NCBI36
NG_042054.1:g.36436C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.1757C= MANE Select	ENSP00000318884.9:p.Ala586=
ENST00000681210.1:c.56C=	ENSP00000505131.1:p.Ala19=
ENST00000681741.1:c.56C=	ENSP00000505116.1:p.Ala19=
ENST00000681824.1:c.56C=	ENSP00000505818.1:p.Ala19=
ENST00000319653.13:c.1757C=	ENSP00000318884.9:p.Ala586=
ENST00000447095.5:c.56C=	ENSP00000409308.1:p.Ala19=
NM_001305424.1:c.1757C=	NP_001292353.1:p.Ala586=
NM_020066.4:c.1757C=	NP_064450.3:p.Ala586=
XM_011544237.1:c.1757C=	XP_011542539.1:p.Ala586=
XR_949151.1:n.1978C=
NM_001348094.1:c.1757C=	NP_001335023.1:p.Ala586=
XM_011544237.3:c.1757C=	XP_011542539.1:p.Ala586=
XM_017001837.1:c.1757C=	XP_016857326.1:p.Ala586=
XM_017001838.1:c.1757C=	XP_016857327.1:p.Ala586=
NM_020066.5:c.1757C= MANE Select	NP_064450.3:p.Ala586=
NM_001305424.2:c.1757C=	NP_001292353.1:p.Ala586=
NM_001348094.2:c.1757C=	NP_001335023.1:p.Ala586=