Canonical Allele Identifier: CA4776285

Gene: SULF1

Linked Data

• dbSNP Id: rs6990375
• ExAC: 8:70571531 G / A
• gnomAD v2: 8-70571531-G-A
• gnomAD v3: 8-69659296-G-A
• gnomAD v4: 8-69659296-G-A
• MyVariant Identifiers: chr8:g.70571531G>A (hg19) ; chr8:g.69659296G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.69659296G>A , CM000670.2:g.69659296G>A	GRCh38
NC_000008.10:g.70571531G>A , CM000670.1:g.70571531G>A	GRCh37
NC_000008.9:g.70734085G>A	NCBI36
NG_042849.1:g.197673G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402687.9:c.*761G>A MANE Select	ENSP00000385704.4:n.*761G>A
ENST00000260128.8:c.*761G>A	ENSP00000260128.4:n.*761G>A
ENST00000402687.8:c.*761G>A	ENSP00000385704.4:n.*761G>A
ENST00000419716.7:c.*761G>A	ENSP00000390315.3:n.*761G>A
ENST00000458141.6:c.*761G>A	ENSP00000403040.2:n.*761G>A
ENST00000521946.5:n.2892G>A
ENST00000530674.1:n.1991G>A
ENST00000531512.5:c.1255G>A
NM_001128204.1:c.*761G>A	NP_001121676.1:n.*761G>A
NM_001128205.1:c.*761G>A	NP_001121677.1:n.*761G>A
NM_001128206.1:c.*761G>A	NP_001121678.1:n.*761G>A
NM_015170.2:c.*761G>A	NP_055985.2:n.*761G>A
NR_132437.1:n.2902G>A
XM_006716438.2:c.3343G>A	XP_006716501.1:p.Ala1115Thr
XM_006716439.2:c.3343G>A	XP_006716502.1:p.Ala1115Thr
XM_006716440.2:c.3343G>A	XP_006716503.1:p.Ala1115Thr
XM_006716441.1:c.2620G>A	XP_006716504.1:p.Ala874Thr
XM_006716442.1:c.*761G>A	XP_006716505.1:n.*761G>A
XM_011517494.1:c.3343G>A	XP_011515796.1:p.Ala1115Thr
XR_928764.1:n.3989G>A
NR_156414.1:n.3795G>A
NR_156415.1:n.3957G>A
XM_006716438.3:c.3343G>A	XP_006716501.1:p.Ala1115Thr
XM_006716439.3:c.3343G>A	XP_006716502.1:p.Ala1115Thr
XM_006716440.3:c.3343G>A	XP_006716503.1:p.Ala1115Thr
XM_011517494.2:c.3343G>A	XP_011515796.1:p.Ala1115Thr
XM_024447112.1:c.*761G>A	XP_024302880.1:n.*761G>A
NM_001128205.2:c.*761G>A MANE Select	NP_001121677.1:n.*761G>A
NM_001128204.2:c.*761G>A	NP_001121676.1:n.*761G>A
NM_001128206.2:c.*761G>A	NP_001121678.1:n.*761G>A
NR_156414.2:n.3741G>A
NR_156415.2:n.3903G>A
NM_015170.3:c.*761G>A	NP_055985.2:n.*761G>A