Canonical Allele Identifier: CA16021275

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98899333C>G , CM000668.2:g.98899333C>G	GRCh38
NC_000006.11:g.99347209C>G , CM000668.1:g.99347209C>G	GRCh37
NC_000006.10:g.99453930C>G	NCBI36
NG_033903.1:g.53674G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001278716.2:c.1252G>C MANE Select	NP_001265645.1:p.Ala418Pro
ENST00000369244.7:c.1252G>C MANE Select	ENSP00000358247.1:p.Ala418Pro
NM_001278716.1:c.1252G>C	NP_001265645.1:p.Ala418Pro
NM_012160.4:c.1252G>C	NP_036292.2:p.Ala418Pro
NM_012160.5:c.1252G>C	NP_036292.2:p.Ala418Pro
NR_103836.1:n.1297G>C
NR_103836.2:n.1237G>C
NR_103837.1:n.1297G>C
NR_103837.2:n.1237G>C
ENST00000229971.2:c.1252G>C	ENSP00000229971.1:p.Ala418Pro
ENST00000369244.6:c.1252G>C	ENSP00000358247.1:p.Ala418Pro
XM_005266930.1:c.1252G>C	XP_005266987.1:p.Ala418Pro
XM_005266930.3:c.1252G>C	XP_005266987.1:p.Ala418Pro
XM_017010726.1:c.1252G>C	XP_016866215.1:p.Ala418Pro
XM_017010727.2:c.1252G>C	XP_016866216.1:p.Ala418Pro
XM_017010728.1:c.526G>C	XP_016866217.1:p.Ala176Pro