Canonical Allele Identifier: CA2222077874
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51136126A= , CM000678.2:g.51136126A= GRCh38
NC_000016.9:g.51170037A= , CM000678.1:g.51170037A= GRCh37
NC_000016.8:g.49727538A= NCBI36
NG_007990.1:g.20147T= , LRG_674:g.20147T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.*986T= ENSP00000407914.2:n.*986T=
ENST00000685868.1:c.*986T= ENSP00000509873.1:n.*986T=
ENST00000251020.9:c.*986T= MANE Select ENSP00000251020.4:n.*986T=
ENST00000251020.8:c.*986T= ENSP00000251020.4:n.*986T=
ENST00000440970.5:c.*986T= ENSP00000407914.1:n.*986T=
NM_001127892.1:c.*986T= NP_001121364.1:n.*986T=
NM_002968.2:c.*986T= , LRG_674t1:c.*986T= NP_002959.2:n.*986T=
XM_006721241.2:c.*986T= XP_006721304.1:n.*986T=
XM_011523254.1:c.*986T= XP_011521556.1:n.*986T=
XM_011523255.1:c.*986T= XP_011521557.1:n.*986T=
NM_002968.3:c.*986T= MANE Select NP_002959.2:n.*986T=
NM_001127892.2:c.*986T= NP_001121364.1:n.*986T=