Canonical Allele Identifier: CA365084782

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99322233G>T (hg19) ; chr6:g.98874357G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874357G>T , CM000668.2:g.98874357G>T	GRCh38
NC_000006.11:g.99322233G>T , CM000668.1:g.99322233G>T	GRCh37
NC_000006.10:g.99428954G>T	NCBI36
NG_033903.1:g.78650C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1787C>A MANE Select	ENSP00000358247.1:p.Ser596Ter
ENST00000229971.2:c.1787C>A	ENSP00000229971.1:p.Ser596Ter
ENST00000369244.6:c.1787C>A	ENSP00000358247.1:p.Ser596Ter
NM_001278716.1:c.1787C>A	NP_001265645.1:p.Ser596Ter
NM_012160.4:c.1787C>A	NP_036292.2:p.Ser596Ter
NR_103836.1:n.1832C>A
XM_005266930.1:c.1715C>A	XP_005266987.1:p.Ser572Ter
XM_005266930.3:c.1715C>A	XP_005266987.1:p.Ser572Ter
XM_017010726.1:c.1787C>A	XP_016866215.1:p.Ser596Ter
XM_017010727.2:c.1715C>A	XP_016866216.1:p.Ser572Ter
XM_017010728.1:c.1061C>A	XP_016866217.1:p.Ser354Ter
NM_001278716.2:c.1787C>A MANE Select	NP_001265645.1:p.Ser596Ter
NR_103836.2:n.1772C>A
NM_012160.5:c.1787C>A	NP_036292.2:p.Ser596Ter