Canonical Allele Identifier: CA530161379
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1247372620

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240378136_240378139del , CM000663.2:g.240378136_240378139del GRCh38
NC_000001.10:g.240541436_240541439del , CM000663.1:g.240541436_240541439del GRCh37
NC_000001.9:g.238608059_238608062del NCBI36
NG_042054.1:g.291252_291255del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14375_4859-14372del MANE Select ENSP00000318884.9:n.4859-14375_4859-14372del
ENST00000545751.3:c.700-14375_700-14372del
ENST00000679390.1:n.1121-14375_1121-14372del
ENST00000679646.1:n.4325-14375_4325-14372del
ENST00000679980.1:c.1128-14375_1128-14372del
ENST00000681131.1:c.859-14375_859-14372del
ENST00000681210.1:c.1079-14375_1079-14372del ENSP00000505131.1:n.1079-14375_1079-14372del
ENST00000681296.1:n.2046-14375_2046-14372del
ENST00000681741.1:c.*903-14375_*903-14372del ENSP00000505116.1:n.*903-14375_*903-14372del
ENST00000681805.1:c.744-14375_744-14372del
ENST00000681824.1:c.986-14375_986-14372del ENSP00000505818.1:n.986-14375_986-14372del
ENST00000319653.13:c.4859-14375_4859-14372del ENSP00000318884.9:n.4859-14375_4859-14372del
ENST00000545751.2:c.287-14375_287-14372del ENSP00000437918.2:n.287-14375_287-14372del
NM_001305424.1:c.4871-14375_4871-14372del NP_001292353.1:n.4871-14375_4871-14372del
NM_020066.4:c.4859-14375_4859-14372del NP_064450.3:n.4859-14375_4859-14372del
NM_001348094.1:c.2687-14375_2687-14372del NP_001335023.1:n.2687-14375_2687-14372del
XM_017001840.2:c.2999-14375_2999-14372del XP_016857329.1:n.2999-14375_2999-14372del
XM_017001841.2:c.2999-14375_2999-14372del XP_016857330.1:n.2999-14375_2999-14372del
NM_020066.5:c.4859-14375_4859-14372del MANE Select NP_064450.3:n.4859-14375_4859-14372del
NM_001305424.2:c.4871-14375_4871-14372del NP_001292353.1:n.4871-14375_4871-14372del
NM_001348094.2:c.2687-14375_2687-14372del NP_001335023.1:n.2687-14375_2687-14372del