Canonical Allele Identifier: CA40315323

Gene: FMN2

Linked Data

• dbSNP Id: rs989301603
• MyVariant Identifiers: chr1:g.240541087_240541091del (hg19) ; chr1:g.240377787_240377791del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377791_240377795del , CM000663.2:g.240377791_240377795del	GRCh38
NC_000001.10:g.240541091_240541095del , CM000663.1:g.240541091_240541095del	GRCh37
NC_000001.9:g.238607714_238607718del	NCBI36
NG_042054.1:g.290907_290911del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-14720_4859-14716del MANE Select	ENSP00000318884.9:n.4859-14720_4859-14716del
ENST00000545751.3:c.700-14720_700-14716del
ENST00000679390.1:n.1121-14720_1121-14716del
ENST00000679646.1:n.4325-14720_4325-14716del
ENST00000679980.1:c.1128-14720_1128-14716del
ENST00000681131.1:c.859-14720_859-14716del
ENST00000681210.1:c.1079-14720_1079-14716del	ENSP00000505131.1:n.1079-14720_1079-14716del
ENST00000681296.1:n.2046-14720_2046-14716del
ENST00000681741.1:c.*903-14720_*903-14716del	ENSP00000505116.1:n.*903-14720_*903-14716del
ENST00000681805.1:c.744-14720_744-14716del
ENST00000681824.1:c.986-14720_986-14716del	ENSP00000505818.1:n.986-14720_986-14716del
ENST00000319653.13:c.4859-14720_4859-14716del	ENSP00000318884.9:n.4859-14720_4859-14716del
ENST00000545751.2:c.287-14720_287-14716del	ENSP00000437918.2:n.287-14720_287-14716del
NM_001305424.1:c.4871-14720_4871-14716del	NP_001292353.1:n.4871-14720_4871-14716del
NM_020066.4:c.4859-14720_4859-14716del	NP_064450.3:n.4859-14720_4859-14716del
NM_001348094.1:c.2687-14720_2687-14716del	NP_001335023.1:n.2687-14720_2687-14716del
XM_017001840.2:c.2999-14720_2999-14716del	XP_016857329.1:n.2999-14720_2999-14716del
XM_017001841.2:c.2999-14720_2999-14716del	XP_016857330.1:n.2999-14720_2999-14716del
NM_020066.5:c.4859-14720_4859-14716del MANE Select	NP_064450.3:n.4859-14720_4859-14716del
NM_001305424.2:c.4871-14720_4871-14716del	NP_001292353.1:n.4871-14720_4871-14716del
NM_001348094.2:c.2687-14720_2687-14716del	NP_001335023.1:n.2687-14720_2687-14716del