Canonical Allele Identifier: CA361654831

Gene: FBXO38

Linked Data

• MyVariant Identifiers: chr5:g.147781640G>C (hg19) ; chr5:g.148402077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148402077G>C , CM000667.2:g.148402077G>C	GRCh38
NC_000005.9:g.147781640G>C , CM000667.1:g.147781640G>C	GRCh37
NC_000005.8:g.147761833G>C	NCBI36
NG_033871.1:g.23143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340253.10:c.358G>C MANE Select	ENSP00000342023.6:p.Val120Leu
ENST00000296701.10:c.358G>C	ENSP00000296701.6:p.Val120Leu
ENST00000340253.9:c.358G>C	ENSP00000342023.5:p.Val120Leu
ENST00000394370.7:c.358G>C	ENSP00000377895.3:p.Val120Leu
ENST00000502629.1:n.232G>C
ENST00000503613.5:n.567G>C
ENST00000508326.5:n.459G>C
ENST00000509699.6:n.423G>C
ENST00000511080.5:n.221+7173G>C
ENST00000513826.1:c.358G>C	ENSP00000426410.1:p.Val120Leu
ENST00000521160.5:n.407G>C
NM_001271723.1:c.358G>C	NP_001258652.1:p.Val120Leu
NM_030793.4:c.358G>C	NP_110420.3:p.Val120Leu
XM_005268513.1:c.358G>C	XP_005268570.1:p.Val120Leu
XM_006714797.1:c.358G>C	XP_006714860.1:p.Val120Leu
NM_205836.2:c.358G>C	NP_995308.1:p.Val120Leu
XM_006714797.2:c.358G>C	XP_006714860.1:p.Val120Leu
XM_011537684.3:c.-990G>C	XP_011535986.1:n.-990G>C
XM_017009899.1:c.-900G>C	XP_016865388.1:n.-900G>C
XM_017009900.2:c.-1149G>C	XP_016865389.1:n.-1149G>C
XM_017009901.2:c.-900G>C	XP_016865390.1:n.-900G>C
XM_017009902.2:c.-990G>C	XP_016865391.1:n.-990G>C
XM_024446223.1:c.358G>C	XP_024301991.1:p.Val120Leu
XR_001742284.1:n.504G>C
NM_030793.5:c.358G>C	NP_110420.3:p.Val120Leu
NM_205836.3:c.358G>C MANE Select	NP_995308.1:p.Val120Leu
NM_001271723.2:c.358G>C	NP_001258652.1:p.Val120Leu