Canonical Allele Identifier: CA410047490
Gene: SCAF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31693357G>A , CM000683.2:g.31693357G>A GRCh38
NC_000021.8:g.33065670G>A , CM000683.1:g.33065670G>A GRCh37
NC_000021.7:g.31987541G>A NCBI36
NG_047173.1:g.43762C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020706.2:c.1450C>T MANE Select NP_065757.1:p.Arg484Ter
ENST00000286835.12:c.1450C>T MANE Select ENSP00000286835.7:p.Arg484Ter
NM_001145444.1:c.1405C>T NP_001138916.1:p.Arg469Ter
NM_001145445.1:c.1450C>T NP_001138917.1:p.Arg484Ter
ENST00000286835.11:c.1450C>T ENSP00000286835.7:p.Arg484Ter
ENST00000399804.5:c.1450C>T ENSP00000382703.1:p.Arg484Ter
ENST00000434667.3:c.1405C>T ENSP00000402377.2:p.Arg469Ter
ENST00000467731.1:n.884C>T
XM_005261017.1:c.1273C>T XP_005261074.1:p.Arg425Ter
XM_005261017.3:c.1273C>T XP_005261074.1:p.Arg425Ter
XM_006724035.1:c.1438C>T XP_006724098.1:p.Arg480Ter
XM_006724035.3:c.1438C>T XP_006724098.1:p.Arg480Ter
XM_006724036.1:c.1438C>T XP_006724099.1:p.Arg480Ter
XM_006724036.3:c.1438C>T XP_006724099.1:p.Arg480Ter
XM_017028415.2:c.1447C>T XP_016883904.1:p.Arg483Ter
XM_017028416.2:c.1447C>T XP_016883905.1:p.Arg483Ter
XM_017028417.1:c.1273C>T XP_016883906.1:p.Arg425Ter