Canonical Allele Identifier: CA3933523
Community Standard Title: NM_001278716.2(FBXL4):c.1104-13G>T
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98899494C>A , CM000668.2:g.98899494C>A GRCh38
NC_000006.11:g.99347370C>A , CM000668.1:g.99347370C>A GRCh37
NC_000006.10:g.99454091C>A NCBI36
NG_033903.1:g.53513G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278716.2:c.1104-13G>T MANE Select NP_001265645.1:n.1104-13G>T
ENST00000369244.7:c.1104-13G>T MANE Select ENSP00000358247.1:n.1104-13G>T
NM_001278716.1:c.1104-13G>T NP_001265645.1:n.1104-13G>T
NM_012160.4:c.1104-13G>T NP_036292.2:n.1104-13G>T
NM_012160.5:c.1104-13G>T NP_036292.2:n.1104-13G>T
NR_103836.1:n.1149-13G>T
NR_103836.2:n.1089-13G>T
NR_103837.1:n.1149-13G>T
NR_103837.2:n.1089-13G>T
ENST00000229971.2:c.1104-13G>T ENSP00000229971.1:n.1104-13G>T
ENST00000369244.6:c.1104-13G>T ENSP00000358247.1:n.1104-13G>T
XM_005266930.1:c.1104-13G>T XP_005266987.1:n.1104-13G>T
XM_005266930.3:c.1104-13G>T XP_005266987.1:n.1104-13G>T
XM_017010726.1:c.1104-13G>T XP_016866215.1:n.1104-13G>T
XM_017010727.2:c.1104-13G>T XP_016866216.1:n.1104-13G>T
XM_017010728.1:c.378-13G>T XP_016866217.1:n.378-13G>T