Canonical Allele Identifier: CA365088949

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98926577-T-C
• MyVariant Identifiers: chr6:g.99374453T>C (hg19) ; chr6:g.98926577T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926577T>C , CM000668.2:g.98926577T>C	GRCh38
NC_000006.11:g.99374453T>C , CM000668.1:g.99374453T>C	GRCh37
NC_000006.10:g.99481174T>C	NCBI36
NG_033903.1:g.26430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.412A>G MANE Select	ENSP00000358247.1:p.Thr138Ala
ENST00000229971.2:c.412A>G	ENSP00000229971.1:p.Thr138Ala
ENST00000369244.6:c.412A>G	ENSP00000358247.1:p.Thr138Ala
NM_001278716.1:c.412A>G	NP_001265645.1:p.Thr138Ala
NM_012160.4:c.412A>G	NP_036292.2:p.Thr138Ala
NR_103836.1:n.803A>G
NR_103837.1:n.803A>G
XM_005266930.1:c.412A>G	XP_005266987.1:p.Thr138Ala
XM_011535748.1:c.412A>G	XP_011534050.1:p.Thr138Ala
XM_005266930.3:c.412A>G	XP_005266987.1:p.Thr138Ala
XM_011535748.3:c.412A>G	XP_011534050.1:p.Thr138Ala
XM_017010726.1:c.412A>G	XP_016866215.1:p.Thr138Ala
XM_017010727.2:c.412A>G	XP_016866216.1:p.Thr138Ala
XM_017010728.1:c.-391A>G	XP_016866217.1:n.-391A>G
NM_001278716.2:c.412A>G MANE Select	NP_001265645.1:p.Thr138Ala
NR_103836.2:n.743A>G
NR_103837.2:n.743A>G
NM_012160.5:c.412A>G	NP_036292.2:p.Thr138Ala