Canonical Allele Identifier: CA2675871915

Gene: FBXO38

Linked Data

• gnomAD v4: 5-148425565-T-TCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425565_148425566insCG , CM000667.2:g.148425565_148425566insCG	GRCh38
NC_000005.9:g.147805128_147805129insCG , CM000667.1:g.147805128_147805129insCG	GRCh37
NC_000005.8:g.147785321_147785322insCG	NCBI36
NG_033871.1:g.46631_46632insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000340253.10:c.1782_1783insCG MANE Select	ENSP00000342023.6:p.Val595ArgfsTer14
ENST00000296701.10:c.1782_1783insCG	ENSP00000296701.6:p.Val595ArgfsTer14
ENST00000340253.9:c.1782_1783insCG	ENSP00000342023.5:p.Val595ArgfsTer14
ENST00000394370.7:c.1782_1783insCG	ENSP00000377895.3:p.Val595ArgfsTer14
ENST00000513826.1:c.1782_1783insCG	ENSP00000426410.1:p.Val595ArgfsTer14
ENST00000514832.1:n.413_414insCG
NM_001271723.1:c.1782_1783insCG	NP_001258652.1:p.Val595ArgfsTer14
NM_030793.4:c.1782_1783insCG	NP_110420.3:p.Val595ArgfsTer14
XM_005268513.1:c.1782_1783insCG	XP_005268570.1:p.Val595ArgfsTer14
XM_006714797.1:c.1782_1783insCG	XP_006714860.1:p.Val595ArgfsTer14
XM_011537683.1:c.684_685insCG	XP_011535985.1:p.Val229ArgfsTer14
XM_011537684.1:c.582_583insCG	XP_011535986.1:p.Val195ArgfsTer14
NM_205836.2:c.1782_1783insCG	NP_995308.1:p.Val595ArgfsTer14
XM_006714797.2:c.1782_1783insCG	XP_006714860.1:p.Val595ArgfsTer14
XM_011537684.3:c.582_583insCG	XP_011535986.1:p.Val195ArgfsTer14
XM_017009899.1:c.684_685insCG	XP_016865388.1:p.Val229ArgfsTer14
XM_017009900.2:c.582_583insCG	XP_016865389.1:p.Val195ArgfsTer14
XM_017009901.2:c.684_685insCG	XP_016865390.1:p.Val229ArgfsTer14
XM_017009902.2:c.582_583insCG	XP_016865391.1:p.Val195ArgfsTer14
XM_024446223.1:c.1782_1783insCG	XP_024301991.1:p.Val595ArgfsTer14
XR_001742284.1:n.1928_1929insCG
NM_030793.5:c.1782_1783insCG	NP_110420.3:p.Val595ArgfsTer14
NM_205836.3:c.1782_1783insCG MANE Select	NP_995308.1:p.Val595ArgfsTer14
NM_001271723.2:c.1782_1783insCG	NP_001258652.1:p.Val595ArgfsTer14