Canonical Allele Identifier: CA2675871913

Gene: FBXO38

Linked Data

• gnomAD v4: 5-148425546-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425549_148425550del , CM000667.2:g.148425549_148425550del	GRCh38
NC_000005.9:g.147805112_147805113del , CM000667.1:g.147805112_147805113del	GRCh37
NC_000005.8:g.147785305_147785306del	NCBI36
NG_033871.1:g.46615_46616del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340253.10:c.1766_1767del MANE Select	ENSP00000342023.6:p.Lys589ThrfsTer8
ENST00000296701.10:c.1766_1767del	ENSP00000296701.6:p.Lys589ThrfsTer8
ENST00000340253.9:c.1766_1767del	ENSP00000342023.5:p.Lys589ThrfsTer8
ENST00000394370.7:c.1766_1767del	ENSP00000377895.3:p.Lys589ThrfsTer8
ENST00000513826.1:c.1766_1767del	ENSP00000426410.1:p.Lys589ThrfsTer8
ENST00000514832.1:n.397_398del
NM_001271723.1:c.1766_1767del	NP_001258652.1:p.Lys589ThrfsTer8
NM_030793.4:c.1766_1767del	NP_110420.3:p.Lys589ThrfsTer8
XM_005268513.1:c.1766_1767del	XP_005268570.1:p.Lys589ThrfsTer8
XM_006714797.1:c.1766_1767del	XP_006714860.1:p.Lys589ThrfsTer8
XM_011537683.1:c.668_669del	XP_011535985.1:p.Lys223ThrfsTer8
XM_011537684.1:c.566_567del	XP_011535986.1:p.Lys189ThrfsTer8
NM_205836.2:c.1766_1767del	NP_995308.1:p.Lys589ThrfsTer8
XM_006714797.2:c.1766_1767del	XP_006714860.1:p.Lys589ThrfsTer8
XM_011537684.3:c.566_567del	XP_011535986.1:p.Lys189ThrfsTer8
XM_017009899.1:c.668_669del	XP_016865388.1:p.Lys223ThrfsTer8
XM_017009900.2:c.566_567del	XP_016865389.1:p.Lys189ThrfsTer8
XM_017009901.2:c.668_669del	XP_016865390.1:p.Lys223ThrfsTer8
XM_017009902.2:c.566_567del	XP_016865391.1:p.Lys189ThrfsTer8
XM_024446223.1:c.1766_1767del	XP_024301991.1:p.Lys589ThrfsTer8
XR_001742284.1:n.1912_1913del
NM_030793.5:c.1766_1767del	NP_110420.3:p.Lys589ThrfsTer8
NM_205836.3:c.1766_1767del MANE Select	NP_995308.1:p.Lys589ThrfsTer8
NM_001271723.2:c.1766_1767del	NP_001258652.1:p.Lys589ThrfsTer8