Canonical Allele Identifier: CA530161372
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1358815012

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377900_240377904del , CM000663.2:g.240377900_240377904del GRCh38
NC_000001.10:g.240541200_240541204del , CM000663.1:g.240541200_240541204del GRCh37
NC_000001.9:g.238607823_238607827del NCBI36
NG_042054.1:g.291016_291020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14611_4859-14607del MANE Select ENSP00000318884.9:n.4859-14611_4859-14607del
ENST00000545751.3:c.700-14611_700-14607del
ENST00000679390.1:n.1121-14611_1121-14607del
ENST00000679646.1:n.4325-14611_4325-14607del
ENST00000679980.1:c.1128-14611_1128-14607del
ENST00000681131.1:c.859-14611_859-14607del
ENST00000681210.1:c.1079-14611_1079-14607del ENSP00000505131.1:n.1079-14611_1079-14607del
ENST00000681296.1:n.2046-14611_2046-14607del
ENST00000681741.1:c.*903-14611_*903-14607del ENSP00000505116.1:n.*903-14611_*903-14607del
ENST00000681805.1:c.744-14611_744-14607del
ENST00000681824.1:c.986-14611_986-14607del ENSP00000505818.1:n.986-14611_986-14607del
ENST00000319653.13:c.4859-14611_4859-14607del ENSP00000318884.9:n.4859-14611_4859-14607del
ENST00000545751.2:c.287-14611_287-14607del ENSP00000437918.2:n.287-14611_287-14607del
NM_001305424.1:c.4871-14611_4871-14607del NP_001292353.1:n.4871-14611_4871-14607del
NM_020066.4:c.4859-14611_4859-14607del NP_064450.3:n.4859-14611_4859-14607del
NM_001348094.1:c.2687-14611_2687-14607del NP_001335023.1:n.2687-14611_2687-14607del
XM_017001840.2:c.2999-14611_2999-14607del XP_016857329.1:n.2999-14611_2999-14607del
XM_017001841.2:c.2999-14611_2999-14607del XP_016857330.1:n.2999-14611_2999-14607del
NM_020066.5:c.4859-14611_4859-14607del MANE Select NP_064450.3:n.4859-14611_4859-14607del
NM_001305424.2:c.4871-14611_4871-14607del NP_001292353.1:n.4871-14611_4871-14607del
NM_001348094.2:c.2687-14611_2687-14607del NP_001335023.1:n.2687-14611_2687-14607del