Canonical Allele Identifier: CA361655364
Gene: FBXO38 HGNC NCBI

Linked Data

dbSNP Id: rs1458391761

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425558C>T , CM000667.2:g.148425558C>T GRCh38
NC_000005.9:g.147805121C>T , CM000667.1:g.147805121C>T GRCh37
NC_000005.8:g.147785314C>T NCBI36
NG_033871.1:g.46624C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340253.10:c.1775C>T MANE Select ENSP00000342023.6:p.Ser592Leu
ENST00000296701.10:c.1775C>T ENSP00000296701.6:p.Ser592Leu
ENST00000340253.9:c.1775C>T ENSP00000342023.5:p.Ser592Leu
ENST00000394370.7:c.1775C>T ENSP00000377895.3:p.Ser592Leu
ENST00000513826.1:c.1775C>T ENSP00000426410.1:p.Ser592Leu
ENST00000514832.1:n.406C>T
NM_001271723.1:c.1775C>T NP_001258652.1:p.Ser592Leu
NM_030793.4:c.1775C>T NP_110420.3:p.Ser592Leu
XM_005268513.1:c.1775C>T XP_005268570.1:p.Ser592Leu
XM_006714797.1:c.1775C>T XP_006714860.1:p.Ser592Leu
XM_011537683.1:c.677C>T XP_011535985.1:p.Ser226Leu
XM_011537684.1:c.575C>T XP_011535986.1:p.Ser192Leu
NM_205836.2:c.1775C>T NP_995308.1:p.Ser592Leu
XM_006714797.2:c.1775C>T XP_006714860.1:p.Ser592Leu
XM_011537684.3:c.575C>T XP_011535986.1:p.Ser192Leu
XM_017009899.1:c.677C>T XP_016865388.1:p.Ser226Leu
XM_017009900.2:c.575C>T XP_016865389.1:p.Ser192Leu
XM_017009901.2:c.677C>T XP_016865390.1:p.Ser226Leu
XM_017009902.2:c.575C>T XP_016865391.1:p.Ser192Leu
XM_024446223.1:c.1775C>T XP_024301991.1:p.Ser592Leu
XR_001742284.1:n.1921C>T
NM_030793.5:c.1775C>T NP_110420.3:p.Ser592Leu
NM_205836.3:c.1775C>T MANE Select NP_995308.1:p.Ser592Leu
NM_001271723.2:c.1775C>T NP_001258652.1:p.Ser592Leu