Canonical Allele Identifier: CA1229115548

Gene: FMN2

Linked Data

• dbSNP Id: rs1673763643

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240396173_240396177del , CM000663.2:g.240396173_240396177del	GRCh38
NC_000001.10:g.240559473_240559477del , CM000663.1:g.240559473_240559477del	GRCh37
NC_000001.9:g.238626096_238626100del	NCBI36
NG_042054.1:g.309289_309293del

Transcript Alleles

HGVS	Amino-acid change
ENST00000319653.14:c.4910+3611_4910+3615del MANE Select	ENSP00000318884.9:n.4910+3611_4910+3615del
ENST00000545751.3:c.751+3611_751+3615del
ENST00000679390.1:n.1172+3611_1172+3615del
ENST00000679646.1:n.4376+3611_4376+3615del
ENST00000679980.1:c.1179+3611_1179+3615del
ENST00000681131.1:c.910+3611_910+3615del
ENST00000681210.1:c.1130+3611_1130+3615del	ENSP00000505131.1:n.1130+3611_1130+3615del
ENST00000681296.1:n.2097+3611_2097+3615del
ENST00000681741.1:c.*954+3611_*954+3615del	ENSP00000505116.1:n.*954+3611_*954+3615del
ENST00000681805.1:c.795+3611_795+3615del
ENST00000681824.1:c.1037+3611_1037+3615del	ENSP00000505818.1:n.1037+3611_1037+3615del
ENST00000319653.13:c.4910+3611_4910+3615del	ENSP00000318884.9:n.4910+3611_4910+3615del
ENST00000545751.2:c.338+3611_338+3615del	ENSP00000437918.2:n.338+3611_338+3615del
NM_001305424.1:c.4922+3611_4922+3615del	NP_001292353.1:n.4922+3611_4922+3615del
NM_020066.4:c.4910+3611_4910+3615del	NP_064450.3:n.4910+3611_4910+3615del
NM_001348094.1:c.2738+3611_2738+3615del	NP_001335023.1:n.2738+3611_2738+3615del
XM_017001840.2:c.3050+3611_3050+3615del	XP_016857329.1:n.3050+3611_3050+3615del
XM_017001841.2:c.3050+3611_3050+3615del	XP_016857330.1:n.3050+3611_3050+3615del
NM_020066.5:c.4910+3611_4910+3615del MANE Select	NP_064450.3:n.4910+3611_4910+3615del
NM_001305424.2:c.4922+3611_4922+3615del	NP_001292353.1:n.4922+3611_4922+3615del
NM_001348094.2:c.2738+3611_2738+3615del	NP_001335023.1:n.2738+3611_2738+3615del