Canonical Allele Identifier: CA1229107858

Gene: FMN2

Linked Data

• dbSNP Id: rs1673101007

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377959_240377960del , CM000663.2:g.240377959_240377960del	GRCh38
NC_000001.10:g.240541259_240541260del , CM000663.1:g.240541259_240541260del	GRCh37
NC_000001.9:g.238607882_238607883del	NCBI36
NG_042054.1:g.291075_291076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14552_4859-14551del MANE Select	ENSP00000318884.9:n.4859-14552_4859-14551del
ENST00000545751.3:c.700-14552_700-14551del
ENST00000679390.1:n.1121-14552_1121-14551del
ENST00000679646.1:n.4325-14552_4325-14551del
ENST00000679980.1:c.1128-14552_1128-14551del
ENST00000681131.1:c.859-14552_859-14551del
ENST00000681210.1:c.1079-14552_1079-14551del	ENSP00000505131.1:n.1079-14552_1079-14551del
ENST00000681296.1:n.2046-14552_2046-14551del
ENST00000681741.1:c.*903-14552_*903-14551del	ENSP00000505116.1:n.*903-14552_*903-14551del
ENST00000681805.1:c.744-14552_744-14551del
ENST00000681824.1:c.986-14552_986-14551del	ENSP00000505818.1:n.986-14552_986-14551del
ENST00000319653.13:c.4859-14552_4859-14551del	ENSP00000318884.9:n.4859-14552_4859-14551del
ENST00000545751.2:c.287-14552_287-14551del	ENSP00000437918.2:n.287-14552_287-14551del
NM_001305424.1:c.4871-14552_4871-14551del	NP_001292353.1:n.4871-14552_4871-14551del
NM_020066.4:c.4859-14552_4859-14551del	NP_064450.3:n.4859-14552_4859-14551del
NM_001348094.1:c.2687-14552_2687-14551del	NP_001335023.1:n.2687-14552_2687-14551del
XM_017001840.2:c.2999-14552_2999-14551del	XP_016857329.1:n.2999-14552_2999-14551del
XM_017001841.2:c.2999-14552_2999-14551del	XP_016857330.1:n.2999-14552_2999-14551del
NM_020066.5:c.4859-14552_4859-14551del MANE Select	NP_064450.3:n.4859-14552_4859-14551del
NM_001305424.2:c.4871-14552_4871-14551del	NP_001292353.1:n.4871-14552_4871-14551del
NM_001348094.2:c.2687-14552_2687-14551del	NP_001335023.1:n.2687-14552_2687-14551del