Canonical Allele Identifier: CA1229107818
Gene: FMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377878_240377889delinsTATTATATTCCC , CM000663.2:g.240377878_240377889delinsTATTATATTCCC GRCh38
NC_000001.10:g.240541178_240541189delinsTATTATATTCCC , CM000663.1:g.240541178_240541189delinsTATTATATTCCC GRCh37
NC_000001.9:g.238607801_238607812delinsTATTATATTCCC NCBI36
NG_042054.1:g.290994_291005delinsTATTATATTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14633_4859-14622delinsTATTATATTCCC MANE Select ENSP00000318884.9:n.4859-14633_4859-14622delinsTATTATATTCCC
ENST00000545751.3:c.700-14633_700-14622delinsTATTATATTCCC
ENST00000679390.1:n.1121-14633_1121-14622delinsTATTATATTCCC
ENST00000679646.1:n.4325-14633_4325-14622delinsTATTATATTCCC
ENST00000679980.1:c.1128-14633_1128-14622delinsTATTATATTCCC
ENST00000681131.1:c.859-14633_859-14622delinsTATTATATTCCC
ENST00000681210.1:c.1079-14633_1079-14622delinsTATTATATTCCC ENSP00000505131.1:n.1079-14633_1079-14622delinsTATTATATTCCC
ENST00000681296.1:n.2046-14633_2046-14622delinsTATTATATTCCC
ENST00000681741.1:c.*903-14633_*903-14622delinsTATTATATTCCC ENSP00000505116.1:n.*903-14633_*903-14622delinsTATTATATTCCC
ENST00000681805.1:c.744-14633_744-14622delinsTATTATATTCCC
ENST00000681824.1:c.986-14633_986-14622delinsTATTATATTCCC ENSP00000505818.1:n.986-14633_986-14622delinsTATTATATTCCC
ENST00000319653.13:c.4859-14633_4859-14622delinsTATTATATTCCC ENSP00000318884.9:n.4859-14633_4859-14622delinsTATTATATTCCC
ENST00000545751.2:c.287-14633_287-14622delinsTATTATATTCCC ENSP00000437918.2:n.287-14633_287-14622delinsTATTATATTCCC
NM_001305424.1:c.4871-14633_4871-14622delinsTATTATATTCCC NP_001292353.1:n.4871-14633_4871-14622delinsTATTATATTCCC
NM_020066.4:c.4859-14633_4859-14622delinsTATTATATTCCC NP_064450.3:n.4859-14633_4859-14622delinsTATTATATTCCC
NM_001348094.1:c.2687-14633_2687-14622delinsTATTATATTCCC NP_001335023.1:n.2687-14633_2687-14622delinsTATTATATTCCC
XM_017001840.2:c.2999-14633_2999-14622delinsTATTATATTCCC XP_016857329.1:n.2999-14633_2999-14622delinsTATTATATTCCC
XM_017001841.2:c.2999-14633_2999-14622delinsTATTATATTCCC XP_016857330.1:n.2999-14633_2999-14622delinsTATTATATTCCC
NM_020066.5:c.4859-14633_4859-14622delinsTATTATATTCCC MANE Select NP_064450.3:n.4859-14633_4859-14622delinsTATTATATTCCC
NM_001305424.2:c.4871-14633_4871-14622delinsTATTATATTCCC NP_001292353.1:n.4871-14633_4871-14622delinsTATTATATTCCC
NM_001348094.2:c.2687-14633_2687-14622delinsTATTATATTCCC NP_001335023.1:n.2687-14633_2687-14622delinsTATTATATTCCC