Canonical Allele Identifier: CA2222078371

Gene: SALL1

Linked Data

• dbSNP Id: rs1962299746

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136452T>C , CM000678.2:g.51136452T>C	GRCh38
NC_000016.9:g.51170363T>C , CM000678.1:g.51170363T>C	GRCh37
NC_000016.8:g.49727864T>C	NCBI36
NG_007990.1:g.19821A>G , LRG_674:g.19821A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.*660A>G	ENSP00000407914.2:n.*660A>G
ENST00000685868.1:c.*660A>G	ENSP00000509873.1:n.*660A>G
ENST00000251020.9:c.*660A>G MANE Select	ENSP00000251020.4:n.*660A>G
ENST00000251020.8:c.*660A>G	ENSP00000251020.4:n.*660A>G
ENST00000440970.5:c.*660A>G	ENSP00000407914.1:n.*660A>G
NM_001127892.1:c.*660A>G	NP_001121364.1:n.*660A>G
NM_002968.2:c.*660A>G , LRG_674t1:c.*660A>G	NP_002959.2:n.*660A>G
XM_006721241.2:c.*660A>G	XP_006721304.1:n.*660A>G
XM_011523254.1:c.*660A>G	XP_011521556.1:n.*660A>G
XM_011523255.1:c.*660A>G	XP_011521557.1:n.*660A>G
NM_002968.3:c.*660A>G MANE Select	NP_002959.2:n.*660A>G
NM_001127892.2:c.*660A>G	NP_001121364.1:n.*660A>G