Canonical Allele Identifier: CA1229107907

Gene: FMN2

Linked Data

• dbSNP Id: rs1430260604

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240378125_240378128dup , CM000663.2:g.240378125_240378128dup	GRCh38
NC_000001.10:g.240541425_240541428dup , CM000663.1:g.240541425_240541428dup	GRCh37
NC_000001.9:g.238608048_238608051dup	NCBI36
NG_042054.1:g.291241_291244dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14386_4859-14383dup MANE Select	ENSP00000318884.9:n.4859-14386_4859-14383dup
ENST00000545751.3:c.700-14386_700-14383dup
ENST00000679390.1:n.1121-14386_1121-14383dup
ENST00000679646.1:n.4325-14386_4325-14383dup
ENST00000679980.1:c.1128-14386_1128-14383dup
ENST00000681131.1:c.859-14386_859-14383dup
ENST00000681210.1:c.1079-14386_1079-14383dup	ENSP00000505131.1:n.1079-14386_1079-14383dup
ENST00000681296.1:n.2046-14386_2046-14383dup
ENST00000681741.1:c.*903-14386_*903-14383dup	ENSP00000505116.1:n.*903-14386_*903-14383dup
ENST00000681805.1:c.744-14386_744-14383dup
ENST00000681824.1:c.986-14386_986-14383dup	ENSP00000505818.1:n.986-14386_986-14383dup
ENST00000319653.13:c.4859-14386_4859-14383dup	ENSP00000318884.9:n.4859-14386_4859-14383dup
ENST00000545751.2:c.287-14386_287-14383dup	ENSP00000437918.2:n.287-14386_287-14383dup
NM_001305424.1:c.4871-14386_4871-14383dup	NP_001292353.1:n.4871-14386_4871-14383dup
NM_020066.4:c.4859-14386_4859-14383dup	NP_064450.3:n.4859-14386_4859-14383dup
NM_001348094.1:c.2687-14386_2687-14383dup	NP_001335023.1:n.2687-14386_2687-14383dup
XM_017001840.2:c.2999-14386_2999-14383dup	XP_016857329.1:n.2999-14386_2999-14383dup
XM_017001841.2:c.2999-14386_2999-14383dup	XP_016857330.1:n.2999-14386_2999-14383dup
NM_020066.5:c.4859-14386_4859-14383dup MANE Select	NP_064450.3:n.4859-14386_4859-14383dup
NM_001305424.2:c.4871-14386_4871-14383dup	NP_001292353.1:n.4871-14386_4871-14383dup
NM_001348094.2:c.2687-14386_2687-14383dup	NP_001335023.1:n.2687-14386_2687-14383dup