Canonical Allele Identifier: CA1477046

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240208042C>T , CM000663.2:g.240208042C>T	GRCh38
NC_000001.10:g.240371342C>T , CM000663.1:g.240371342C>T	GRCh37
NC_000001.9:g.238437965C>T	NCBI36
NG_042054.1:g.121158C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020066.5:c.3230C>T MANE Select	NP_064450.3:p.Pro1077Leu
ENST00000319653.14:c.3230C>T MANE Select	ENSP00000318884.9:p.Pro1077Leu
NM_001305424.1:c.3242C>T	NP_001292353.1:p.Pro1081Leu
NM_001305424.2:c.3242C>T	NP_001292353.1:p.Pro1081Leu
NM_001348094.1:c.1986+19780C>T	NP_001335023.1:n.1986+19780C>T
NM_001348094.2:c.1986+19780C>T	NP_001335023.1:n.1986+19780C>T
NM_020066.4:c.3230C>T	NP_064450.3:p.Pro1077Leu
ENST00000319653.13:c.3230C>T	ENSP00000318884.9:p.Pro1077Leu
ENST00000545751.3:c.56+19780C>T
ENST00000679980.1:c.189+1050C>T
ENST00000681210.1:c.285+19780C>T	ENSP00000505131.1:n.285+19780C>T
ENST00000681741.1:c.286-3049C>T	ENSP00000505116.1:n.286-3049C>T
ENST00000681824.1:c.285+19780C>T	ENSP00000505818.1:n.285+19780C>T
XM_011544237.1:c.3242C>T	XP_011542539.1:p.Pro1081Leu
XM_011544237.3:c.3242C>T	XP_011542539.1:p.Pro1081Leu
XM_017001837.1:c.3242C>T	XP_016857326.1:p.Pro1081Leu
XM_017001838.1:c.3242C>T	XP_016857327.1:p.Pro1081Leu
XM_017001840.2:c.1370C>T	XP_016857329.1:p.Pro457Leu
XM_017001841.2:c.1370C>T	XP_016857330.1:p.Pro457Leu
XR_949151.1:n.3463C>T