Canonical Allele Identifier: CA3497089

Gene: FBXO38

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148404733A>G , CM000667.2:g.148404733A>G	GRCh38
NC_000005.9:g.147784296A>G , CM000667.1:g.147784296A>G	GRCh37
NC_000005.8:g.147764489A>G	NCBI36
NG_033871.1:g.25799A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_205836.3:c.641A>G MANE Select	NP_995308.1:p.Tyr214Cys
ENST00000340253.10:c.641A>G MANE Select	ENSP00000342023.6:p.Tyr214Cys
NM_001271723.1:c.641A>G	NP_001258652.1:p.Tyr214Cys
NM_001271723.2:c.641A>G	NP_001258652.1:p.Tyr214Cys
NM_030793.4:c.641A>G	NP_110420.3:p.Tyr214Cys
NM_030793.5:c.641A>G	NP_110420.3:p.Tyr214Cys
NM_205836.2:c.641A>G	NP_995308.1:p.Tyr214Cys
ENST00000296701.10:c.641A>G	ENSP00000296701.6:p.Tyr214Cys
ENST00000340253.9:c.641A>G	ENSP00000342023.5:p.Tyr214Cys
ENST00000394370.7:c.641A>G	ENSP00000377895.3:p.Tyr214Cys
ENST00000502571.1:n.50A>G
ENST00000509699.6:n.706A>G
ENST00000511080.5:n.221+9829A>G
ENST00000513826.1:c.641A>G	ENSP00000426410.1:p.Tyr214Cys
XM_005268513.1:c.641A>G	XP_005268570.1:p.Tyr214Cys
XM_006714797.1:c.641A>G	XP_006714860.1:p.Tyr214Cys
XM_006714797.2:c.641A>G	XP_006714860.1:p.Tyr214Cys
XM_011537684.3:c.-707A>G	XP_011535986.1:n.-707A>G
XM_017009899.1:c.-617A>G	XP_016865388.1:n.-617A>G
XM_017009900.2:c.-866A>G	XP_016865389.1:n.-866A>G
XM_017009901.2:c.-617A>G	XP_016865390.1:n.-617A>G
XM_017009902.2:c.-707A>G	XP_016865391.1:n.-707A>G
XM_024446223.1:c.641A>G	XP_024301991.1:p.Tyr214Cys
XR_001742284.1:n.787A>G