Canonical Allele Identifier: CA1590037568

Gene: FBXO38

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425627C= , CM000667.2:g.148425627C=	GRCh38
NC_000005.9:g.147805190C= , CM000667.1:g.147805190C=	GRCh37
NC_000005.8:g.147785383C=	NCBI36
NG_033871.1:g.46693C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340253.10:c.1844C= MANE Select	ENSP00000342023.6:p.Pro615=
ENST00000296701.10:c.1844C=	ENSP00000296701.6:p.Pro615=
ENST00000340253.9:c.1844C=	ENSP00000342023.5:p.Pro615=
ENST00000394370.7:c.1844C=	ENSP00000377895.3:p.Pro615=
ENST00000513826.1:c.1844C=	ENSP00000426410.1:p.Pro615=
ENST00000514832.1:n.475C=
NM_001271723.1:c.1844C=	NP_001258652.1:p.Pro615=
NM_030793.4:c.1844C=	NP_110420.3:p.Pro615=
XM_005268513.1:c.1844C=	XP_005268570.1:p.Pro615=
XM_006714797.1:c.1844C=	XP_006714860.1:p.Pro615=
XM_011537683.1:c.746C=	XP_011535985.1:p.Pro249=
XM_011537684.1:c.644C=	XP_011535986.1:p.Pro215=
NM_205836.2:c.1844C=	NP_995308.1:p.Pro615=
XM_006714797.2:c.1844C=	XP_006714860.1:p.Pro615=
XM_011537684.3:c.644C=	XP_011535986.1:p.Pro215=
XM_017009899.1:c.746C=	XP_016865388.1:p.Pro249=
XM_017009900.2:c.644C=	XP_016865389.1:p.Pro215=
XM_017009901.2:c.746C=	XP_016865390.1:p.Pro249=
XM_017009902.2:c.644C=	XP_016865391.1:p.Pro215=
XM_024446223.1:c.1844C=	XP_024301991.1:p.Pro615=
XR_001742284.1:n.1990C=
NM_030793.5:c.1844C=	NP_110420.3:p.Pro615=
NM_205836.3:c.1844C= MANE Select	NP_995308.1:p.Pro615=
NM_001271723.2:c.1844C=	NP_001258652.1:p.Pro615=