Canonical Allele Identifier: CA1228998426

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240123434T= , CM000663.2:g.240123434T=	GRCh38
NC_000001.10:g.240286734T= , CM000663.1:g.240286734T=	GRCh37
NC_000001.9:g.238353357T=	NCBI36
NG_042054.1:g.36550T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.1782+89T= MANE Select	ENSP00000318884.9:n.1782+89T=
ENST00000681210.1:c.81+89T=	ENSP00000505131.1:n.81+89T=
ENST00000681741.1:c.81+89T=	ENSP00000505116.1:n.81+89T=
ENST00000681824.1:c.81+89T=	ENSP00000505818.1:n.81+89T=
ENST00000319653.13:c.1782+89T=	ENSP00000318884.9:n.1782+89T=
ENST00000447095.5:c.81+89T=	ENSP00000409308.1:n.81+89T=
NM_001305424.1:c.1782+89T=	NP_001292353.1:n.1782+89T=
NM_020066.4:c.1782+89T=	NP_064450.3:n.1782+89T=
XM_011544237.1:c.1782+89T=	XP_011542539.1:n.1782+89T=
XR_949151.1:n.2003+89T=
NM_001348094.1:c.1782+89T=	NP_001335023.1:n.1782+89T=
XM_011544237.3:c.1782+89T=	XP_011542539.1:n.1782+89T=
XM_017001837.1:c.1782+89T=	XP_016857326.1:n.1782+89T=
XM_017001838.1:c.1782+89T=	XP_016857327.1:n.1782+89T=
NM_020066.5:c.1782+89T= MANE Select	NP_064450.3:n.1782+89T=
NM_001305424.2:c.1782+89T=	NP_001292353.1:n.1782+89T=
NM_001348094.2:c.1782+89T=	NP_001335023.1:n.1782+89T=