Canonical Allele Identifier: CA395891949

Gene: SALL1

Linked Data

• gnomAD v4: 16-51141776-G-C
• MyVariant Identifiers: chr16:g.51175687G>C (hg19) ; chr16:g.51141776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141776G>C , CM000678.2:g.51141776G>C	GRCh38
NC_000016.9:g.51175687G>C , CM000678.1:g.51175687G>C	GRCh37
NC_000016.8:g.49733188G>C	NCBI36
NG_007990.1:g.14497C>G , LRG_674:g.14497C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.446C>G	ENSP00000407914.2:p.Pro149Arg
ENST00000570206.2:c.155C>G	ENSP00000456777.2:p.Pro52Arg
ENST00000685868.1:c.446C>G	ENSP00000509873.1:p.Pro149Arg
ENST00000690502.1:c.446C>G	ENSP00000510560.1:p.Pro149Arg
ENST00000251020.9:c.446C>G MANE Select	ENSP00000251020.4:p.Pro149Arg
ENST00000251020.8:c.446C>G	ENSP00000251020.4:p.Pro149Arg
ENST00000440970.5:c.155C>G	ENSP00000407914.1:p.Pro52Arg
ENST00000566102.1:c.77-4224C>G	ENSP00000455582.1:n.77-4224C>G
ENST00000570206.1:c.155C>G	ENSP00000456777.1:p.Pro52Arg
NM_001127892.1:c.155C>G	NP_001121364.1:p.Pro52Arg
NM_002968.2:c.446C>G , LRG_674t1:c.446C>G	NP_002959.2:p.Pro149Arg
XM_006721241.2:c.446C>G	XP_006721304.1:p.Pro149Arg
XM_011523254.1:c.446C>G	XP_011521556.1:p.Pro149Arg
XM_011523255.1:c.446C>G	XP_011521557.1:p.Pro149Arg
NM_002968.3:c.446C>G MANE Select	NP_002959.2:p.Pro149Arg
NM_001127892.2:c.155C>G	NP_001121364.1:p.Pro52Arg