Canonical Allele Identifier: CA40315361
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs751104290

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240378161_240378163dup , CM000663.2:g.240378161_240378163dup GRCh38
NC_000001.10:g.240541461_240541463dup , CM000663.1:g.240541461_240541463dup GRCh37
NC_000001.9:g.238608084_238608086dup NCBI36
NG_042054.1:g.291277_291279dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14350_4859-14348dup MANE Select ENSP00000318884.9:n.4859-14350_4859-14348dup
ENST00000545751.3:c.700-14350_700-14348dup
ENST00000679390.1:n.1121-14350_1121-14348dup
ENST00000679646.1:n.4325-14350_4325-14348dup
ENST00000679980.1:c.1128-14350_1128-14348dup
ENST00000681131.1:c.859-14350_859-14348dup
ENST00000681210.1:c.1079-14350_1079-14348dup ENSP00000505131.1:n.1079-14350_1079-14348dup
ENST00000681296.1:n.2046-14350_2046-14348dup
ENST00000681741.1:c.*903-14350_*903-14348dup ENSP00000505116.1:n.*903-14350_*903-14348dup
ENST00000681805.1:c.744-14350_744-14348dup
ENST00000681824.1:c.986-14350_986-14348dup ENSP00000505818.1:n.986-14350_986-14348dup
ENST00000319653.13:c.4859-14350_4859-14348dup ENSP00000318884.9:n.4859-14350_4859-14348dup
ENST00000545751.2:c.287-14350_287-14348dup ENSP00000437918.2:n.287-14350_287-14348dup
NM_001305424.1:c.4871-14350_4871-14348dup NP_001292353.1:n.4871-14350_4871-14348dup
NM_020066.4:c.4859-14350_4859-14348dup NP_064450.3:n.4859-14350_4859-14348dup
NM_001348094.1:c.2687-14350_2687-14348dup NP_001335023.1:n.2687-14350_2687-14348dup
XM_017001840.2:c.2999-14350_2999-14348dup XP_016857329.1:n.2999-14350_2999-14348dup
XM_017001841.2:c.2999-14350_2999-14348dup XP_016857330.1:n.2999-14350_2999-14348dup
NM_020066.5:c.4859-14350_4859-14348dup MANE Select NP_064450.3:n.4859-14350_4859-14348dup
NM_001305424.2:c.4871-14350_4871-14348dup NP_001292353.1:n.4871-14350_4871-14348dup
NM_001348094.2:c.2687-14350_2687-14348dup NP_001335023.1:n.2687-14350_2687-14348dup