Canonical Allele Identifier: CA2222078120

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136290_51136291delinsCA , CM000678.2:g.51136290_51136291delinsCA	GRCh38
NC_000016.9:g.51170201_51170202delinsCA , CM000678.1:g.51170201_51170202delinsCA	GRCh37
NC_000016.8:g.49727702_49727703delinsCA	NCBI36
NG_007990.1:g.19982_19983delinsTG , LRG_674:g.19982_19983delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.*821_*822delinsTG	ENSP00000407914.2:n.*821_*822delinsTG
ENST00000685868.1:c.*821_*822delinsTG	ENSP00000509873.1:n.*821_*822delinsTG
ENST00000251020.9:c.*821_*822delinsTG MANE Select	ENSP00000251020.4:n.*821_*822delinsTG
ENST00000251020.8:c.*821_*822delinsTG	ENSP00000251020.4:n.*821_*822delinsTG
ENST00000440970.5:c.*821_*822delinsTG	ENSP00000407914.1:n.*821_*822delinsTG
NM_001127892.1:c.*821_*822delinsTG	NP_001121364.1:n.*821_*822delinsTG
NM_002968.2:c.*821_*822delinsTG , LRG_674t1:c.*821_*822delinsTG	NP_002959.2:n.*821_*822delinsTG
XM_006721241.2:c.*821_*822delinsTG	XP_006721304.1:n.*821_*822delinsTG
XM_011523254.1:c.*821_*822delinsTG	XP_011521556.1:n.*821_*822delinsTG
XM_011523255.1:c.*821_*822delinsTG	XP_011521557.1:n.*821_*822delinsTG
NM_002968.3:c.*821_*822delinsTG MANE Select	NP_002959.2:n.*821_*822delinsTG
NM_001127892.2:c.*821_*822delinsTG	NP_001121364.1:n.*821_*822delinsTG