Canonical Allele Identifier: CA1229107726
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1673090162

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377638_240377650dup , CM000663.2:g.240377638_240377650dup GRCh38
NC_000001.10:g.240540938_240540950dup , CM000663.1:g.240540938_240540950dup GRCh37
NC_000001.9:g.238607561_238607573dup NCBI36
NG_042054.1:g.290754_290766dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14873_4859-14861dup MANE Select ENSP00000318884.9:n.4859-14873_4859-14861dup
ENST00000545751.3:c.700-14873_700-14861dup
ENST00000679390.1:n.1121-14873_1121-14861dup
ENST00000679646.1:n.4325-14873_4325-14861dup
ENST00000679980.1:c.1128-14873_1128-14861dup
ENST00000681131.1:c.859-14873_859-14861dup
ENST00000681210.1:c.1079-14873_1079-14861dup ENSP00000505131.1:n.1079-14873_1079-14861dup
ENST00000681296.1:n.2046-14873_2046-14861dup
ENST00000681741.1:c.*903-14873_*903-14861dup ENSP00000505116.1:n.*903-14873_*903-14861dup
ENST00000681805.1:c.744-14873_744-14861dup
ENST00000681824.1:c.986-14873_986-14861dup ENSP00000505818.1:n.986-14873_986-14861dup
ENST00000319653.13:c.4859-14873_4859-14861dup ENSP00000318884.9:n.4859-14873_4859-14861dup
ENST00000545751.2:c.287-14873_287-14861dup ENSP00000437918.2:n.287-14873_287-14861dup
NM_001305424.1:c.4871-14873_4871-14861dup NP_001292353.1:n.4871-14873_4871-14861dup
NM_020066.4:c.4859-14873_4859-14861dup NP_064450.3:n.4859-14873_4859-14861dup
NM_001348094.1:c.2687-14873_2687-14861dup NP_001335023.1:n.2687-14873_2687-14861dup
XM_017001840.2:c.2999-14873_2999-14861dup XP_016857329.1:n.2999-14873_2999-14861dup
XM_017001841.2:c.2999-14873_2999-14861dup XP_016857330.1:n.2999-14873_2999-14861dup
NM_020066.5:c.4859-14873_4859-14861dup MANE Select NP_064450.3:n.4859-14873_4859-14861dup
NM_001305424.2:c.4871-14873_4871-14861dup NP_001292353.1:n.4871-14873_4871-14861dup
NM_001348094.2:c.2687-14873_2687-14861dup NP_001335023.1:n.2687-14873_2687-14861dup