Canonical Allele Identifier: CA2222077795

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136083_51136088delinsCCCTTT , CM000678.2:g.51136083_51136088delinsCCCTTT	GRCh38
NC_000016.9:g.51169994_51169999delinsCCCTTT , CM000678.1:g.51169994_51169999delinsCCCTTT	GRCh37
NC_000016.8:g.49727495_49727500delinsCCCTTT	NCBI36
NG_007990.1:g.20185_20190delinsAAAGGG , LRG_674:g.20185_20190delinsAAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.*1024_*1029delinsAAAGGG	ENSP00000407914.2:n.*1024_*1029delinsAAAGGG
ENST00000685868.1:c.*1024_*1029delinsAAAGGG	ENSP00000509873.1:n.*1024_*1029delinsAAAGGG
ENST00000251020.9:c.*1024_*1029delinsAAAGGG MANE Select	ENSP00000251020.4:n.*1024_*1029delinsAAAGGG
ENST00000251020.8:c.*1024_*1029delinsAAAGGG	ENSP00000251020.4:n.*1024_*1029delinsAAAGGG
ENST00000440970.5:c.*1024_*1029delinsAAAGGG	ENSP00000407914.1:n.*1024_*1029delinsAAAGGG
NM_001127892.1:c.*1024_*1029delinsAAAGGG	NP_001121364.1:n.*1024_*1029delinsAAAGGG
NM_002968.2:c.*1024_*1029delinsAAAGGG , LRG_674t1:c.*1024_*1029delinsAAAGGG	NP_002959.2:n.*1024_*1029delinsAAAGGG
XM_006721241.2:c.*1024_*1029delinsAAAGGG	XP_006721304.1:n.*1024_*1029delinsAAAGGG
XM_011523254.1:c.*1024_*1029delinsAAAGGG	XP_011521556.1:n.*1024_*1029delinsAAAGGG
XM_011523255.1:c.*1024_*1029delinsAAAGGG	XP_011521557.1:n.*1024_*1029delinsAAAGGG
NM_002968.3:c.*1024_*1029delinsAAAGGG MANE Select	NP_002959.2:n.*1024_*1029delinsAAAGGG
NM_001127892.2:c.*1024_*1029delinsAAAGGG	NP_001121364.1:n.*1024_*1029delinsAAAGGG