Canonical Allele Identifier: CA128949035

Gene: FBXO38

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425711T>C , CM000667.2:g.148425711T>C	GRCh38
NC_000005.9:g.147805274T>C , CM000667.1:g.147805274T>C	GRCh37
NC_000005.8:g.147785467T>C	NCBI36
NG_033871.1:g.46777T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_205836.3:c.1918+10T>C MANE Select	NP_995308.1:n.1918+10T>C
ENST00000340253.10:c.1918+10T>C MANE Select	ENSP00000342023.6:n.1918+10T>C
NM_001271723.1:c.1918+10T>C	NP_001258652.1:n.1918+10T>C
NM_001271723.2:c.1918+10T>C	NP_001258652.1:n.1918+10T>C
NM_030793.4:c.1918+10T>C	NP_110420.3:n.1918+10T>C
NM_030793.5:c.1918+10T>C	NP_110420.3:n.1918+10T>C
NM_205836.2:c.1918+10T>C	NP_995308.1:n.1918+10T>C
ENST00000296701.10:c.1918+10T>C	ENSP00000296701.6:n.1918+10T>C
ENST00000340253.9:c.1918+10T>C	ENSP00000342023.5:n.1918+10T>C
ENST00000394370.7:c.1918+10T>C	ENSP00000377895.3:n.1918+10T>C
ENST00000513826.1:c.1918+10T>C	ENSP00000426410.1:n.1918+10T>C
ENST00000514832.1:n.549+10T>C
XM_005268513.1:c.1918+10T>C	XP_005268570.1:n.1918+10T>C
XM_006714797.1:c.1918+10T>C	XP_006714860.1:n.1918+10T>C
XM_006714797.2:c.1918+10T>C	XP_006714860.1:n.1918+10T>C
XM_011537683.1:c.820+10T>C	XP_011535985.1:n.820+10T>C
XM_011537684.1:c.718+10T>C	XP_011535986.1:n.718+10T>C
XM_011537684.3:c.718+10T>C	XP_011535986.1:n.718+10T>C
XM_017009899.1:c.820+10T>C	XP_016865388.1:n.820+10T>C
XM_017009900.2:c.718+10T>C	XP_016865389.1:n.718+10T>C
XM_017009901.2:c.820+10T>C	XP_016865390.1:n.820+10T>C
XM_017009902.2:c.718+10T>C	XP_016865391.1:n.718+10T>C
XM_024446223.1:c.1918+10T>C	XP_024301991.1:n.1918+10T>C
XR_001742284.1:n.2064+10T>C