Canonical Allele Identifier: CA2807012906
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51139369_51139370insCCT , CM000678.2:g.51139369_51139370insCCT GRCh38
NC_000016.9:g.51173280_51173281insCCT , CM000678.1:g.51173280_51173281insCCT GRCh37
NC_000016.8:g.49730781_49730782insCCT NCBI36
NG_007990.1:g.16903_16904insAGG , LRG_674:g.16903_16904insAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.2852_2853insAGG ENSP00000407914.2:p.Ala951_Val952insGly
ENST00000570206.2:c.2561_2562insAGG ENSP00000456777.2:p.Ala854_Val855insGly
ENST00000685868.1:c.2852_2853insAGG ENSP00000509873.1:p.Ala951_Val952insGly
ENST00000690502.1:c.2852_2853insAGG ENSP00000510560.1:p.Ala951_Val952insGly
ENST00000251020.9:c.2852_2853insAGG MANE Select ENSP00000251020.4:p.Ala951_Val952insGly
ENST00000251020.8:c.2852_2853insAGG ENSP00000251020.4:p.Ala951_Val952insGly
ENST00000440970.5:c.2561_2562insAGG ENSP00000407914.1:p.Ala854_Val855insGly
ENST00000566102.1:c.77-1818_77-1817insAGG ENSP00000455582.1:n.77-1818_77-1817insAGG
ENST00000570206.1:c.2561_2562insAGG ENSP00000456777.1:p.Ala854_Val855insGly
NM_001127892.1:c.2561_2562insAGG NP_001121364.1:p.Ala854_Val855insGly
NM_002968.2:c.2852_2853insAGG , LRG_674t1:c.2852_2853insAGG NP_002959.2:p.Ala951_Val952insGly
XM_006721241.2:c.2852_2853insAGG XP_006721304.1:p.Ala951_Val952insGly
XM_011523254.1:c.2852_2853insAGG XP_011521556.1:p.Ala951_Val952insGly
XM_011523255.1:c.2852_2853insAGG XP_011521557.1:p.Ala951_Val952insGly
NM_002968.3:c.2852_2853insAGG MANE Select NP_002959.2:p.Ala951_Val952insGly
NM_001127892.2:c.2561_2562insAGG NP_001121364.1:p.Ala854_Val855insGly