Canonical Allele Identifier: CA645592646

Gene: SALL1

Linked Data

• COSMIC: COSM4566179

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51138992_51138993delinsAT , CM000678.2:g.51138992_51138993delinsAT	GRCh38
NC_000016.9:g.51172903_51172904delinsAT , CM000678.1:g.51172903_51172904delinsAT	GRCh37
NC_000016.8:g.49730404_49730405delinsAT	NCBI36
NG_007990.1:g.17280_17281delinsAT , LRG_674:g.17280_17281delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.3229_3230delinsAT	ENSP00000407914.2:p.Pro1077Ile
ENST00000570206.2:c.2938_2939delinsAT	ENSP00000456777.2:p.Pro980Ile
ENST00000685868.1:c.3229_3230delinsAT	ENSP00000509873.1:p.Pro1077Ile
ENST00000690502.1:c.3229_3230delinsAT	ENSP00000510560.1:p.Pro1077Ile
ENST00000251020.9:c.3229_3230delinsAT MANE Select	ENSP00000251020.4:p.Pro1077Ile
ENST00000251020.8:c.3229_3230delinsAT	ENSP00000251020.4:p.Pro1077Ile
ENST00000440970.5:c.2938_2939delinsAT	ENSP00000407914.1:p.Pro980Ile
ENST00000566102.1:c.77-1441_77-1440delinsAT	ENSP00000455582.1:n.77-1441_77-1440delinsAT
ENST00000570206.1:c.2938_2939delinsAT	ENSP00000456777.1:p.Pro980Ile
NM_001127892.1:c.2938_2939delinsAT	NP_001121364.1:p.Pro980Ile
NM_002968.2:c.3229_3230delinsAT , LRG_674t1:c.3229_3230delinsAT	NP_002959.2:p.Pro1077Ile
XM_006721241.2:c.3229_3230delinsAT	XP_006721304.1:p.Pro1077Ile
XM_011523254.1:c.3229_3230delinsAT	XP_011521556.1:p.Pro1077Ile
XM_011523255.1:c.3229_3230delinsAT	XP_011521557.1:p.Pro1077Ile
NM_002968.3:c.3229_3230delinsAT MANE Select	NP_002959.2:p.Pro1077Ile
NM_001127892.2:c.2938_2939delinsAT	NP_001121364.1:p.Pro980Ile