Canonical Allele Identifier: CA345430954

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240093163G>T , CM000663.2:g.240093163G>T	GRCh38
NC_000001.10:g.240256463G>T , CM000663.1:g.240256463G>T	GRCh37
NC_000001.9:g.238323086G>T	NCBI36
NG_042054.1:g.6279G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020066.5:c.1054G>T MANE Select	NP_064450.3:p.Asp352Tyr
ENST00000319653.14:c.1054G>T MANE Select	ENSP00000318884.9:p.Asp352Tyr
NM_001305424.1:c.1054G>T	NP_001292353.1:p.Asp352Tyr
NM_001305424.2:c.1054G>T	NP_001292353.1:p.Asp352Tyr
NM_001348094.1:c.1054G>T	NP_001335023.1:p.Asp352Tyr
NM_001348094.2:c.1054G>T	NP_001335023.1:p.Asp352Tyr
NM_020066.4:c.1054G>T	NP_064450.3:p.Asp352Tyr
ENST00000319653.13:c.1054G>T	ENSP00000318884.9:p.Asp352Tyr
ENST00000447095.5:c.-87+25090G>T	ENSP00000409308.1:n.-87+25090G>T
XM_011544237.1:c.1054G>T	XP_011542539.1:p.Asp352Tyr
XM_011544237.3:c.1054G>T	XP_011542539.1:p.Asp352Tyr
XM_017001837.1:c.1054G>T	XP_016857326.1:p.Asp352Tyr
XM_017001838.1:c.1054G>T	XP_016857327.1:p.Asp352Tyr
XR_949151.1:n.1275G>T