Canonical Allele Identifier: CA530161206
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1460326823

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377508_240377510del , CM000663.2:g.240377508_240377510del GRCh38
NC_000001.10:g.240540808_240540810del , CM000663.1:g.240540808_240540810del GRCh37
NC_000001.9:g.238607431_238607433del NCBI36
NG_042054.1:g.290624_290626del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-15003_4859-15001del MANE Select ENSP00000318884.9:n.4859-15003_4859-15001del
ENST00000545751.3:c.700-15003_700-15001del
ENST00000679390.1:n.1121-15003_1121-15001del
ENST00000679646.1:n.4325-15003_4325-15001del
ENST00000679980.1:c.1128-15003_1128-15001del
ENST00000681131.1:c.859-15003_859-15001del
ENST00000681210.1:c.1079-15003_1079-15001del ENSP00000505131.1:n.1079-15003_1079-15001del
ENST00000681296.1:n.2046-15003_2046-15001del
ENST00000681741.1:c.*903-15003_*903-15001del ENSP00000505116.1:n.*903-15003_*903-15001del
ENST00000681805.1:c.744-15003_744-15001del
ENST00000681824.1:c.986-15003_986-15001del ENSP00000505818.1:n.986-15003_986-15001del
ENST00000319653.13:c.4859-15003_4859-15001del ENSP00000318884.9:n.4859-15003_4859-15001del
ENST00000545751.2:c.287-15003_287-15001del ENSP00000437918.2:n.287-15003_287-15001del
NM_001305424.1:c.4871-15003_4871-15001del NP_001292353.1:n.4871-15003_4871-15001del
NM_020066.4:c.4859-15003_4859-15001del NP_064450.3:n.4859-15003_4859-15001del
NM_001348094.1:c.2687-15003_2687-15001del NP_001335023.1:n.2687-15003_2687-15001del
XM_017001840.2:c.2999-15003_2999-15001del XP_016857329.1:n.2999-15003_2999-15001del
XM_017001841.2:c.2999-15003_2999-15001del XP_016857330.1:n.2999-15003_2999-15001del
NM_020066.5:c.4859-15003_4859-15001del MANE Select NP_064450.3:n.4859-15003_4859-15001del
NM_001305424.2:c.4871-15003_4871-15001del NP_001292353.1:n.4871-15003_4871-15001del
NM_001348094.2:c.2687-15003_2687-15001del NP_001335023.1:n.2687-15003_2687-15001del