Canonical Allele Identifier: CA365084711

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99322212A>C (hg19) ; chr6:g.98874336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874336A>C , CM000668.2:g.98874336A>C	GRCh38
NC_000006.11:g.99322212A>C , CM000668.1:g.99322212A>C	GRCh37
NC_000006.10:g.99428933A>C	NCBI36
NG_033903.1:g.78671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1808T>G MANE Select	ENSP00000358247.1:p.Val603Gly
ENST00000229971.2:c.1808T>G	ENSP00000229971.1:p.Val603Gly
ENST00000369244.6:c.1808T>G	ENSP00000358247.1:p.Val603Gly
NM_001278716.1:c.1808T>G	NP_001265645.1:p.Val603Gly
NM_012160.4:c.1808T>G	NP_036292.2:p.Val603Gly
NR_103836.1:n.1853T>G
XM_005266930.1:c.1736T>G	XP_005266987.1:p.Val579Gly
XM_005266930.3:c.1736T>G	XP_005266987.1:p.Val579Gly
XM_017010726.1:c.1808T>G	XP_016866215.1:p.Val603Gly
XM_017010727.2:c.1736T>G	XP_016866216.1:p.Val579Gly
XM_017010728.1:c.1082T>G	XP_016866217.1:p.Val361Gly
NM_001278716.2:c.1808T>G MANE Select	NP_001265645.1:p.Val603Gly
NR_103836.2:n.1793T>G
NM_012160.5:c.1808T>G	NP_036292.2:p.Val603Gly