Canonical Allele Identifier: CA3933628

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98917497A>G , CM000668.2:g.98917497A>G	GRCh38
NC_000006.11:g.99365373A>G , CM000668.1:g.99365373A>G	GRCh37
NC_000006.10:g.99472094A>G	NCBI36
NG_033903.1:g.35510T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001278716.2:c.735T>C MANE Select	NP_001265645.1:p.Asp245=
ENST00000369244.7:c.735T>C MANE Select	ENSP00000358247.1:p.Asp245=
NM_001278716.1:c.735T>C	NP_001265645.1:p.Asp245=
NM_012160.4:c.735T>C	NP_036292.2:p.Asp245=
NM_012160.5:c.735T>C	NP_036292.2:p.Asp245=
NR_103836.1:n.903+8980T>C
NR_103836.2:n.843+8980T>C
NR_103837.1:n.903+8980T>C
NR_103837.2:n.843+8980T>C
ENST00000229971.2:c.735T>C	ENSP00000229971.1:p.Asp245=
ENST00000369244.6:c.735T>C	ENSP00000358247.1:p.Asp245=
XM_005266930.1:c.735T>C	XP_005266987.1:p.Asp245=
XM_005266930.3:c.735T>C	XP_005266987.1:p.Asp245=
XM_011535748.1:c.735T>C	XP_011534050.1:p.Asp245=
XM_011535748.3:c.735T>C	XP_011534050.1:p.Asp245=
XM_017010726.1:c.735T>C	XP_016866215.1:p.Asp245=
XM_017010727.2:c.735T>C	XP_016866216.1:p.Asp245=
XM_017010728.1:c.9T>C	XP_016866217.1:p.Asp3=