Canonical Allele Identifier: CA1229107645

Gene: FMN2

Linked Data

• dbSNP Id: rs1673085410

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377497_240377503dup , CM000663.2:g.240377497_240377503dup	GRCh38
NC_000001.10:g.240540797_240540803dup , CM000663.1:g.240540797_240540803dup	GRCh37
NC_000001.9:g.238607420_238607426dup	NCBI36
NG_042054.1:g.290613_290619dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-15014_4859-15008dup MANE Select	ENSP00000318884.9:n.4859-15014_4859-15008dup
ENST00000545751.3:c.700-15014_700-15008dup
ENST00000679390.1:n.1121-15014_1121-15008dup
ENST00000679646.1:n.4325-15014_4325-15008dup
ENST00000679980.1:c.1128-15014_1128-15008dup
ENST00000681131.1:c.859-15014_859-15008dup
ENST00000681210.1:c.1079-15014_1079-15008dup	ENSP00000505131.1:n.1079-15014_1079-15008dup
ENST00000681296.1:n.2046-15014_2046-15008dup
ENST00000681741.1:c.*903-15014_*903-15008dup	ENSP00000505116.1:n.*903-15014_*903-15008dup
ENST00000681805.1:c.744-15014_744-15008dup
ENST00000681824.1:c.986-15014_986-15008dup	ENSP00000505818.1:n.986-15014_986-15008dup
ENST00000319653.13:c.4859-15014_4859-15008dup	ENSP00000318884.9:n.4859-15014_4859-15008dup
ENST00000545751.2:c.287-15014_287-15008dup	ENSP00000437918.2:n.287-15014_287-15008dup
NM_001305424.1:c.4871-15014_4871-15008dup	NP_001292353.1:n.4871-15014_4871-15008dup
NM_020066.4:c.4859-15014_4859-15008dup	NP_064450.3:n.4859-15014_4859-15008dup
NM_001348094.1:c.2687-15014_2687-15008dup	NP_001335023.1:n.2687-15014_2687-15008dup
XM_017001840.2:c.2999-15014_2999-15008dup	XP_016857329.1:n.2999-15014_2999-15008dup
XM_017001841.2:c.2999-15014_2999-15008dup	XP_016857330.1:n.2999-15014_2999-15008dup
NM_020066.5:c.4859-15014_4859-15008dup MANE Select	NP_064450.3:n.4859-15014_4859-15008dup
NM_001305424.2:c.4871-15014_4871-15008dup	NP_001292353.1:n.4871-15014_4871-15008dup
NM_001348094.2:c.2687-15014_2687-15008dup	NP_001335023.1:n.2687-15014_2687-15008dup