Canonical Allele Identifier: CA1229107904

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240378119_240378123delinsCTCTT , CM000663.2:g.240378119_240378123delinsCTCTT	GRCh38
NC_000001.10:g.240541419_240541423delinsCTCTT , CM000663.1:g.240541419_240541423delinsCTCTT	GRCh37
NC_000001.9:g.238608042_238608046delinsCTCTT	NCBI36
NG_042054.1:g.291235_291239delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14392_4859-14388delinsCTCTT MANE Select	ENSP00000318884.9:n.4859-14392_4859-14388delinsCTCTT
ENST00000545751.3:c.700-14392_700-14388delinsCTCTT
ENST00000679390.1:n.1121-14392_1121-14388delinsCTCTT
ENST00000679646.1:n.4325-14392_4325-14388delinsCTCTT
ENST00000679980.1:c.1128-14392_1128-14388delinsCTCTT
ENST00000681131.1:c.859-14392_859-14388delinsCTCTT
ENST00000681210.1:c.1079-14392_1079-14388delinsCTCTT	ENSP00000505131.1:n.1079-14392_1079-14388delinsCTCTT
ENST00000681296.1:n.2046-14392_2046-14388delinsCTCTT
ENST00000681741.1:c.*903-14392_*903-14388delinsCTCTT	ENSP00000505116.1:n.*903-14392_*903-14388delinsCTCTT
ENST00000681805.1:c.744-14392_744-14388delinsCTCTT
ENST00000681824.1:c.986-14392_986-14388delinsCTCTT	ENSP00000505818.1:n.986-14392_986-14388delinsCTCTT
ENST00000319653.13:c.4859-14392_4859-14388delinsCTCTT	ENSP00000318884.9:n.4859-14392_4859-14388delinsCTCTT
ENST00000545751.2:c.287-14392_287-14388delinsCTCTT	ENSP00000437918.2:n.287-14392_287-14388delinsCTCTT
NM_001305424.1:c.4871-14392_4871-14388delinsCTCTT	NP_001292353.1:n.4871-14392_4871-14388delinsCTCTT
NM_020066.4:c.4859-14392_4859-14388delinsCTCTT	NP_064450.3:n.4859-14392_4859-14388delinsCTCTT
NM_001348094.1:c.2687-14392_2687-14388delinsCTCTT	NP_001335023.1:n.2687-14392_2687-14388delinsCTCTT
XM_017001840.2:c.2999-14392_2999-14388delinsCTCTT	XP_016857329.1:n.2999-14392_2999-14388delinsCTCTT
XM_017001841.2:c.2999-14392_2999-14388delinsCTCTT	XP_016857330.1:n.2999-14392_2999-14388delinsCTCTT
NM_020066.5:c.4859-14392_4859-14388delinsCTCTT MANE Select	NP_064450.3:n.4859-14392_4859-14388delinsCTCTT
NM_001305424.2:c.4871-14392_4871-14388delinsCTCTT	NP_001292353.1:n.4871-14392_4871-14388delinsCTCTT
NM_001348094.2:c.2687-14392_2687-14388delinsCTCTT	NP_001335023.1:n.2687-14392_2687-14388delinsCTCTT