Canonical Allele Identifier: CA2580098555

Gene: SCAF4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31671903_31671908del , CM000683.2:g.31671903_31671908del	GRCh38
NC_000021.8:g.33044216_33044221del , CM000683.1:g.33044216_33044221del	GRCh37
NC_000021.7:g.31966087_31966092del	NCBI36
NG_047173.1:g.65215_65220del

Transcript Alleles

HGVS	Amino-acid Change
NM_020706.2:c.2939_2944del MANE Select	NP_065757.1:p.Pro980_Gln981del
ENST00000286835.12:c.2939_2944del MANE Select	ENSP00000286835.7:p.Pro980_Gln981del
NM_001145444.1:c.2894_2899del	NP_001138916.1:p.Pro965_Gln966del
NM_001145445.1:c.2873_2878del	NP_001138917.1:p.Pro958_Gln959del
ENST00000286835.11:c.2939_2944del	ENSP00000286835.7:p.Pro980_Gln981del
ENST00000399804.5:c.2873_2878del	ENSP00000382703.1:p.Pro958_Gln959del
ENST00000434667.3:c.2894_2899del	ENSP00000402377.2:p.Pro965_Gln966del
XM_005261017.1:c.2762_2767del	XP_005261074.1:p.Pro921_Gln922del
XM_005261017.3:c.2762_2767del	XP_005261074.1:p.Pro921_Gln922del
XM_006724035.1:c.2927_2932del	XP_006724098.1:p.Pro976_Gln977del
XM_006724035.3:c.2927_2932del	XP_006724098.1:p.Pro976_Gln977del
XM_006724036.1:c.2861_2866del	XP_006724099.1:p.Pro954_Gln955del
XM_006724036.3:c.2861_2866del	XP_006724099.1:p.Pro954_Gln955del
XM_017028415.2:c.2936_2941del	XP_016883904.1:p.Pro979_Gln980del
XM_017028416.2:c.2870_2875del	XP_016883905.1:p.Pro957_Gln958del
XM_017028417.1:c.2696_2701del	XP_016883906.1:p.Pro899_Gln900del