Canonical Allele Identifier: CA1229107911

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240378128_240378132delinsTTTTG , CM000663.2:g.240378128_240378132delinsTTTTG	GRCh38
NC_000001.10:g.240541428_240541432delinsTTTTG , CM000663.1:g.240541428_240541432delinsTTTTG	GRCh37
NC_000001.9:g.238608051_238608055delinsTTTTG	NCBI36
NG_042054.1:g.291244_291248delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14383_4859-14379delinsTTTTG MANE Select	ENSP00000318884.9:n.4859-14383_4859-14379delinsTTTTG
ENST00000545751.3:c.700-14383_700-14379delinsTTTTG
ENST00000679390.1:n.1121-14383_1121-14379delinsTTTTG
ENST00000679646.1:n.4325-14383_4325-14379delinsTTTTG
ENST00000679980.1:c.1128-14383_1128-14379delinsTTTTG
ENST00000681131.1:c.859-14383_859-14379delinsTTTTG
ENST00000681210.1:c.1079-14383_1079-14379delinsTTTTG	ENSP00000505131.1:n.1079-14383_1079-14379delinsTTTTG
ENST00000681296.1:n.2046-14383_2046-14379delinsTTTTG
ENST00000681741.1:c.*903-14383_*903-14379delinsTTTTG	ENSP00000505116.1:n.*903-14383_*903-14379delinsTTTTG
ENST00000681805.1:c.744-14383_744-14379delinsTTTTG
ENST00000681824.1:c.986-14383_986-14379delinsTTTTG	ENSP00000505818.1:n.986-14383_986-14379delinsTTTTG
ENST00000319653.13:c.4859-14383_4859-14379delinsTTTTG	ENSP00000318884.9:n.4859-14383_4859-14379delinsTTTTG
ENST00000545751.2:c.287-14383_287-14379delinsTTTTG	ENSP00000437918.2:n.287-14383_287-14379delinsTTTTG
NM_001305424.1:c.4871-14383_4871-14379delinsTTTTG	NP_001292353.1:n.4871-14383_4871-14379delinsTTTTG
NM_020066.4:c.4859-14383_4859-14379delinsTTTTG	NP_064450.3:n.4859-14383_4859-14379delinsTTTTG
NM_001348094.1:c.2687-14383_2687-14379delinsTTTTG	NP_001335023.1:n.2687-14383_2687-14379delinsTTTTG
XM_017001840.2:c.2999-14383_2999-14379delinsTTTTG	XP_016857329.1:n.2999-14383_2999-14379delinsTTTTG
XM_017001841.2:c.2999-14383_2999-14379delinsTTTTG	XP_016857330.1:n.2999-14383_2999-14379delinsTTTTG
NM_020066.5:c.4859-14383_4859-14379delinsTTTTG MANE Select	NP_064450.3:n.4859-14383_4859-14379delinsTTTTG
NM_001305424.2:c.4871-14383_4871-14379delinsTTTTG	NP_001292353.1:n.4871-14383_4871-14379delinsTTTTG
NM_001348094.2:c.2687-14383_2687-14379delinsTTTTG	NP_001335023.1:n.2687-14383_2687-14379delinsTTTTG