Canonical Allele Identifier: CA2607482118

Gene: FMN2

Linked Data

• gnomAD v3: 1-240123394-A-ATAGCAGCTACGATGTGTATCTGCCCAGTCACCCTATAATTTAAAAACAACATGTGATTC
• gnomAD v4: 1-240123394-A-ATAGCAGCTACGATGTGTATCTGCCCAGTCACCCTATAATTTAAAAACAACATGTGATTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240123395_240123453dup , CM000663.2:g.240123395_240123453dup	GRCh38
NC_000001.10:g.240286695_240286753dup , CM000663.1:g.240286695_240286753dup	GRCh37
NC_000001.9:g.238353318_238353376dup	NCBI36
NG_042054.1:g.36511_36569dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.1782+50_1782+108dup MANE Select	ENSP00000318884.9:n.1782+50_1782+108dup
ENST00000681210.1:c.81+50_81+108dup	ENSP00000505131.1:n.81+50_81+108dup
ENST00000681741.1:c.81+50_81+108dup	ENSP00000505116.1:n.81+50_81+108dup
ENST00000681824.1:c.81+50_81+108dup	ENSP00000505818.1:n.81+50_81+108dup
ENST00000319653.13:c.1782+50_1782+108dup	ENSP00000318884.9:n.1782+50_1782+108dup
ENST00000447095.5:c.81+50_81+108dup	ENSP00000409308.1:n.81+50_81+108dup
NM_001305424.1:c.1782+50_1782+108dup	NP_001292353.1:n.1782+50_1782+108dup
NM_020066.4:c.1782+50_1782+108dup	NP_064450.3:n.1782+50_1782+108dup
XM_011544237.1:c.1782+50_1782+108dup	XP_011542539.1:n.1782+50_1782+108dup
XR_949151.1:n.2003+50_2003+108dup
NM_001348094.1:c.1782+50_1782+108dup	NP_001335023.1:n.1782+50_1782+108dup
XM_011544237.3:c.1782+50_1782+108dup	XP_011542539.1:n.1782+50_1782+108dup
XM_017001837.1:c.1782+50_1782+108dup	XP_016857326.1:n.1782+50_1782+108dup
XM_017001838.1:c.1782+50_1782+108dup	XP_016857327.1:n.1782+50_1782+108dup
NM_020066.5:c.1782+50_1782+108dup MANE Select	NP_064450.3:n.1782+50_1782+108dup
NM_001305424.2:c.1782+50_1782+108dup	NP_001292353.1:n.1782+50_1782+108dup
NM_001348094.2:c.1782+50_1782+108dup	NP_001335023.1:n.1782+50_1782+108dup