Canonical Allele Identifier: CA2222078044
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51136251T= , CM000678.2:g.51136251T= GRCh38
NC_000016.9:g.51170162T= , CM000678.1:g.51170162T= GRCh37
NC_000016.8:g.49727663T= NCBI36
NG_007990.1:g.20022A= , LRG_674:g.20022A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.*861A= ENSP00000407914.2:n.*861A=
ENST00000685868.1:c.*861A= ENSP00000509873.1:n.*861A=
ENST00000251020.9:c.*861A= MANE Select ENSP00000251020.4:n.*861A=
ENST00000251020.8:c.*861A= ENSP00000251020.4:n.*861A=
ENST00000440970.5:c.*861A= ENSP00000407914.1:n.*861A=
NM_001127892.1:c.*861A= NP_001121364.1:n.*861A=
NM_002968.2:c.*861A= , LRG_674t1:c.*861A= NP_002959.2:n.*861A=
XM_006721241.2:c.*861A= XP_006721304.1:n.*861A=
XM_011523254.1:c.*861A= XP_011521556.1:n.*861A=
XM_011523255.1:c.*861A= XP_011521557.1:n.*861A=
NM_002968.3:c.*861A= MANE Select NP_002959.2:n.*861A=
NM_001127892.2:c.*861A= NP_001121364.1:n.*861A=