Canonical Allele Identifier: CA530161368
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1359477170

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377882_240377886del , CM000663.2:g.240377882_240377886del GRCh38
NC_000001.10:g.240541182_240541186del , CM000663.1:g.240541182_240541186del GRCh37
NC_000001.9:g.238607805_238607809del NCBI36
NG_042054.1:g.290998_291002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14629_4859-14625del MANE Select ENSP00000318884.9:n.4859-14629_4859-14625del
ENST00000545751.3:c.700-14629_700-14625del
ENST00000679390.1:n.1121-14629_1121-14625del
ENST00000679646.1:n.4325-14629_4325-14625del
ENST00000679980.1:c.1128-14629_1128-14625del
ENST00000681131.1:c.859-14629_859-14625del
ENST00000681210.1:c.1079-14629_1079-14625del ENSP00000505131.1:n.1079-14629_1079-14625del
ENST00000681296.1:n.2046-14629_2046-14625del
ENST00000681741.1:c.*903-14629_*903-14625del ENSP00000505116.1:n.*903-14629_*903-14625del
ENST00000681805.1:c.744-14629_744-14625del
ENST00000681824.1:c.986-14629_986-14625del ENSP00000505818.1:n.986-14629_986-14625del
ENST00000319653.13:c.4859-14629_4859-14625del ENSP00000318884.9:n.4859-14629_4859-14625del
ENST00000545751.2:c.287-14629_287-14625del ENSP00000437918.2:n.287-14629_287-14625del
NM_001305424.1:c.4871-14629_4871-14625del NP_001292353.1:n.4871-14629_4871-14625del
NM_020066.4:c.4859-14629_4859-14625del NP_064450.3:n.4859-14629_4859-14625del
NM_001348094.1:c.2687-14629_2687-14625del NP_001335023.1:n.2687-14629_2687-14625del
XM_017001840.2:c.2999-14629_2999-14625del XP_016857329.1:n.2999-14629_2999-14625del
XM_017001841.2:c.2999-14629_2999-14625del XP_016857330.1:n.2999-14629_2999-14625del
NM_020066.5:c.4859-14629_4859-14625del MANE Select NP_064450.3:n.4859-14629_4859-14625del
NM_001305424.2:c.4871-14629_4871-14625del NP_001292353.1:n.4871-14629_4871-14625del
NM_001348094.2:c.2687-14629_2687-14625del NP_001335023.1:n.2687-14629_2687-14625del