Canonical Allele Identifier: CA365088954

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374456G>A (hg19) ; chr6:g.98926580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926580G>A , CM000668.2:g.98926580G>A	GRCh38
NC_000006.11:g.99374456G>A , CM000668.1:g.99374456G>A	GRCh37
NC_000006.10:g.99481177G>A	NCBI36
NG_033903.1:g.26427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.409C>T MANE Select	ENSP00000358247.1:p.Pro137Ser
ENST00000229971.2:c.409C>T	ENSP00000229971.1:p.Pro137Ser
ENST00000369244.6:c.409C>T	ENSP00000358247.1:p.Pro137Ser
NM_001278716.1:c.409C>T	NP_001265645.1:p.Pro137Ser
NM_012160.4:c.409C>T	NP_036292.2:p.Pro137Ser
NR_103836.1:n.800C>T
NR_103837.1:n.800C>T
XM_005266930.1:c.409C>T	XP_005266987.1:p.Pro137Ser
XM_011535748.1:c.409C>T	XP_011534050.1:p.Pro137Ser
XM_005266930.3:c.409C>T	XP_005266987.1:p.Pro137Ser
XM_011535748.3:c.409C>T	XP_011534050.1:p.Pro137Ser
XM_017010726.1:c.409C>T	XP_016866215.1:p.Pro137Ser
XM_017010727.2:c.409C>T	XP_016866216.1:p.Pro137Ser
XM_017010728.1:c.-394C>T	XP_016866217.1:n.-394C>T
NM_001278716.2:c.409C>T MANE Select	NP_001265645.1:p.Pro137Ser
NR_103836.2:n.740C>T
NR_103837.2:n.740C>T
NM_012160.5:c.409C>T	NP_036292.2:p.Pro137Ser