Canonical Allele Identifier: CA1229107831
Gene: FMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240377902_240377903delinsAT , CM000663.2:g.240377902_240377903delinsAT GRCh38
NC_000001.10:g.240541202_240541203delinsAT , CM000663.1:g.240541202_240541203delinsAT GRCh37
NC_000001.9:g.238607825_238607826delinsAT NCBI36
NG_042054.1:g.291018_291019delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4859-14609_4859-14608delinsAT MANE Select ENSP00000318884.9:n.4859-14609_4859-14608delinsAT
ENST00000545751.3:c.700-14609_700-14608delinsAT
ENST00000679390.1:n.1121-14609_1121-14608delinsAT
ENST00000679646.1:n.4325-14609_4325-14608delinsAT
ENST00000679980.1:c.1128-14609_1128-14608delinsAT
ENST00000681131.1:c.859-14609_859-14608delinsAT
ENST00000681210.1:c.1079-14609_1079-14608delinsAT ENSP00000505131.1:n.1079-14609_1079-14608delinsAT
ENST00000681296.1:n.2046-14609_2046-14608delinsAT
ENST00000681741.1:c.*903-14609_*903-14608delinsAT ENSP00000505116.1:n.*903-14609_*903-14608delinsAT
ENST00000681805.1:c.744-14609_744-14608delinsAT
ENST00000681824.1:c.986-14609_986-14608delinsAT ENSP00000505818.1:n.986-14609_986-14608delinsAT
ENST00000319653.13:c.4859-14609_4859-14608delinsAT ENSP00000318884.9:n.4859-14609_4859-14608delinsAT
ENST00000545751.2:c.287-14609_287-14608delinsAT ENSP00000437918.2:n.287-14609_287-14608delinsAT
NM_001305424.1:c.4871-14609_4871-14608delinsAT NP_001292353.1:n.4871-14609_4871-14608delinsAT
NM_020066.4:c.4859-14609_4859-14608delinsAT NP_064450.3:n.4859-14609_4859-14608delinsAT
NM_001348094.1:c.2687-14609_2687-14608delinsAT NP_001335023.1:n.2687-14609_2687-14608delinsAT
XM_017001840.2:c.2999-14609_2999-14608delinsAT XP_016857329.1:n.2999-14609_2999-14608delinsAT
XM_017001841.2:c.2999-14609_2999-14608delinsAT XP_016857330.1:n.2999-14609_2999-14608delinsAT
NM_020066.5:c.4859-14609_4859-14608delinsAT MANE Select NP_064450.3:n.4859-14609_4859-14608delinsAT
NM_001305424.2:c.4871-14609_4871-14608delinsAT NP_001292353.1:n.4871-14609_4871-14608delinsAT
NM_001348094.2:c.2687-14609_2687-14608delinsAT NP_001335023.1:n.2687-14609_2687-14608delinsAT