Canonical Allele Identifier: CA10648530

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136409_51136410del , CM000678.2:g.51136409_51136410del	GRCh38
NC_000016.9:g.51170320_51170321del , CM000678.1:g.51170320_51170321del	GRCh37
NC_000016.8:g.49727821_49727822del	NCBI36
NG_007990.1:g.19866_19867del , LRG_674:g.19866_19867del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.*705_*706del	ENSP00000407914.2:n.*705_*706del
ENST00000685868.1:c.*705_*706del	ENSP00000509873.1:n.*705_*706del
ENST00000251020.9:c.*705_*706del MANE Select	ENSP00000251020.4:n.*705_*706del
ENST00000251020.8:c.*705_*706del	ENSP00000251020.4:n.*705_*706del
ENST00000440970.5:c.*705_*706del	ENSP00000407914.1:n.*705_*706del
NM_001127892.1:c.*705_*706del	NP_001121364.1:n.*705_*706del
NM_002968.2:c.*705_*706del , LRG_674t1:c.*705_*706del	NP_002959.2:n.*705_*706del
XM_006721241.2:c.*705_*706del	XP_006721304.1:n.*705_*706del
XM_011523254.1:c.*705_*706del	XP_011521556.1:n.*705_*706del
XM_011523255.1:c.*705_*706del	XP_011521557.1:n.*705_*706del
NM_002968.3:c.*705_*706del MANE Select	NP_002959.2:n.*705_*706del
NM_001127892.2:c.*705_*706del	NP_001121364.1:n.*705_*706del