Canonical Allele Identifier: CA1013934538

Gene: FMN2

Linked Data

• dbSNP Id: rs1673084159
• gnomAD v3: 1-240377437-TAAAAC-T
• gnomAD v4: 1-240377437-TAAAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377440_240377444del , CM000663.2:g.240377440_240377444del	GRCh38
NC_000001.10:g.240540740_240540744del , CM000663.1:g.240540740_240540744del	GRCh37
NC_000001.9:g.238607363_238607367del	NCBI36
NG_042054.1:g.290556_290560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-15071_4859-15067del MANE Select	ENSP00000318884.9:n.4859-15071_4859-15067del
ENST00000545751.3:c.700-15071_700-15067del
ENST00000679390.1:n.1121-15071_1121-15067del
ENST00000679646.1:n.4325-15071_4325-15067del
ENST00000679980.1:c.1128-15071_1128-15067del
ENST00000681131.1:c.859-15071_859-15067del
ENST00000681210.1:c.1079-15071_1079-15067del	ENSP00000505131.1:n.1079-15071_1079-15067del
ENST00000681296.1:n.2046-15071_2046-15067del
ENST00000681741.1:c.*903-15071_*903-15067del	ENSP00000505116.1:n.*903-15071_*903-15067del
ENST00000681805.1:c.744-15071_744-15067del
ENST00000681824.1:c.986-15071_986-15067del	ENSP00000505818.1:n.986-15071_986-15067del
ENST00000319653.13:c.4859-15071_4859-15067del	ENSP00000318884.9:n.4859-15071_4859-15067del
ENST00000545751.2:c.287-15071_287-15067del	ENSP00000437918.2:n.287-15071_287-15067del
NM_001305424.1:c.4871-15071_4871-15067del	NP_001292353.1:n.4871-15071_4871-15067del
NM_020066.4:c.4859-15071_4859-15067del	NP_064450.3:n.4859-15071_4859-15067del
NM_001348094.1:c.2687-15071_2687-15067del	NP_001335023.1:n.2687-15071_2687-15067del
XM_017001840.2:c.2999-15071_2999-15067del	XP_016857329.1:n.2999-15071_2999-15067del
XM_017001841.2:c.2999-15071_2999-15067del	XP_016857330.1:n.2999-15071_2999-15067del
NM_020066.5:c.4859-15071_4859-15067del MANE Select	NP_064450.3:n.4859-15071_4859-15067del
NM_001305424.2:c.4871-15071_4871-15067del	NP_001292353.1:n.4871-15071_4871-15067del
NM_001348094.2:c.2687-15071_2687-15067del	NP_001335023.1:n.2687-15071_2687-15067del