Canonical Allele Identifier: CA1229115545
Gene: FMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240396166C= , CM000663.2:g.240396166C= GRCh38
NC_000001.10:g.240559466C= , CM000663.1:g.240559466C= GRCh37
NC_000001.9:g.238626089C= NCBI36
NG_042054.1:g.309282C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4910+3604C= MANE Select ENSP00000318884.9:n.4910+3604C=
ENST00000545751.3:c.751+3604C=
ENST00000679390.1:n.1172+3604C=
ENST00000679646.1:n.4376+3604C=
ENST00000679980.1:c.1179+3604C=
ENST00000681131.1:c.910+3604C=
ENST00000681210.1:c.1130+3604C= ENSP00000505131.1:n.1130+3604C=
ENST00000681296.1:n.2097+3604C=
ENST00000681741.1:c.*954+3604C= ENSP00000505116.1:n.*954+3604C=
ENST00000681805.1:c.795+3604C=
ENST00000681824.1:c.1037+3604C= ENSP00000505818.1:n.1037+3604C=
ENST00000319653.13:c.4910+3604C= ENSP00000318884.9:n.4910+3604C=
ENST00000545751.2:c.338+3604C= ENSP00000437918.2:n.338+3604C=
NM_001305424.1:c.4922+3604C= NP_001292353.1:n.4922+3604C=
NM_020066.4:c.4910+3604C= NP_064450.3:n.4910+3604C=
NM_001348094.1:c.2738+3604C= NP_001335023.1:n.2738+3604C=
XM_017001840.2:c.3050+3604C= XP_016857329.1:n.3050+3604C=
XM_017001841.2:c.3050+3604C= XP_016857330.1:n.3050+3604C=
NM_020066.5:c.4910+3604C= MANE Select NP_064450.3:n.4910+3604C=
NM_001305424.2:c.4922+3604C= NP_001292353.1:n.4922+3604C=
NM_001348094.2:c.2738+3604C= NP_001335023.1:n.2738+3604C=