Canonical Allele Identifier: CA410051169

Gene: SCAF4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31703803T>C , CM000683.2:g.31703803T>C	GRCh38
NC_000021.8:g.33076116T>C , CM000683.1:g.33076116T>C	GRCh37
NC_000021.7:g.31997987T>C	NCBI36
NG_047173.1:g.33316A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020706.2:c.283A>G MANE Select	NP_065757.1:p.Thr95Ala
ENST00000286835.12:c.283A>G MANE Select	ENSP00000286835.7:p.Thr95Ala
NM_001145444.1:c.238A>G	NP_001138916.1:p.Thr80Ala
NM_001145445.1:c.283A>G	NP_001138917.1:p.Thr95Ala
ENST00000286835.11:c.283A>G	ENSP00000286835.7:p.Thr95Ala
ENST00000399804.5:c.283A>G	ENSP00000382703.1:p.Thr95Ala
ENST00000434667.3:c.238A>G	ENSP00000402377.2:p.Thr80Ala
ENST00000485790.1:n.552A>G
XM_005261017.1:c.283A>G	XP_005261074.1:p.Thr95Ala
XM_005261017.3:c.283A>G	XP_005261074.1:p.Thr95Ala
XM_006724035.1:c.283A>G	XP_006724098.1:p.Thr95Ala
XM_006724035.3:c.283A>G	XP_006724098.1:p.Thr95Ala
XM_006724036.1:c.283A>G	XP_006724099.1:p.Thr95Ala
XM_006724036.3:c.283A>G	XP_006724099.1:p.Thr95Ala
XM_017028415.2:c.283A>G	XP_016883904.1:p.Thr95Ala
XM_017028416.2:c.283A>G	XP_016883905.1:p.Thr95Ala
XM_017028417.1:c.283A>G	XP_016883906.1:p.Thr95Ala