Canonical Allele Identifier: CA12880875
Gene: SULF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.69605800A>G , CM000670.2:g.69605800A>G GRCh38
NC_000008.10:g.70518035A>G , CM000670.1:g.70518035A>G GRCh37
NC_000008.9:g.70680589A>G NCBI36
NG_042849.1:g.144177A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000402687.9:c.1377+868A>G MANE Select ENSP00000385704.4:n.1377+868A>G
ENST00000260128.8:c.1377+868A>G ENSP00000260128.4:n.1377+868A>G
ENST00000402687.8:c.1377+868A>G ENSP00000385704.4:n.1377+868A>G
ENST00000419716.7:c.1377+868A>G ENSP00000390315.3:n.1377+868A>G
ENST00000458141.6:c.1377+868A>G ENSP00000403040.2:n.1377+868A>G
ENST00000521946.5:n.717+868A>G
ENST00000616868.1:c.729+868A>G ENSP00000480454.1:n.729+868A>G
NM_001128204.1:c.1377+868A>G NP_001121676.1:n.1377+868A>G
NM_001128205.1:c.1377+868A>G NP_001121677.1:n.1377+868A>G
NM_001128206.1:c.1377+868A>G NP_001121678.1:n.1377+868A>G
NM_015170.2:c.1377+868A>G NP_055985.2:n.1377+868A>G
NR_132437.1:n.727+868A>G
XM_006716438.2:c.1377+868A>G XP_006716501.1:n.1377+868A>G
XM_006716439.2:c.1377+868A>G XP_006716502.1:n.1377+868A>G
XM_006716440.2:c.1377+868A>G XP_006716503.1:n.1377+868A>G
XM_006716441.1:c.654+868A>G XP_006716504.1:n.654+868A>G
XM_006716442.1:c.654+868A>G XP_006716505.1:n.654+868A>G
XM_011517494.1:c.1377+868A>G XP_011515796.1:n.1377+868A>G
XM_011517495.1:c.1377+868A>G XP_011515797.1:n.1377+868A>G
XR_928764.1:n.2132+868A>G
NR_156414.1:n.1938+868A>G
NR_156415.1:n.2100+868A>G
XM_006716438.3:c.1377+868A>G XP_006716501.1:n.1377+868A>G
XM_006716439.3:c.1377+868A>G XP_006716502.1:n.1377+868A>G
XM_006716440.3:c.1377+868A>G XP_006716503.1:n.1377+868A>G
XM_011517494.2:c.1377+868A>G XP_011515796.1:n.1377+868A>G
XM_011517495.2:c.1377+868A>G XP_011515797.1:n.1377+868A>G
XM_017013250.2:c.1377+868A>G XP_016868739.1:n.1377+868A>G
XM_024447112.1:c.1377+868A>G XP_024302880.1:n.1377+868A>G
NM_001128205.2:c.1377+868A>G MANE Select NP_001121677.1:n.1377+868A>G
NM_001128204.2:c.1377+868A>G NP_001121676.1:n.1377+868A>G
NM_001128206.2:c.1377+868A>G NP_001121678.1:n.1377+868A>G
NR_156414.2:n.1884+868A>G
NR_156415.2:n.2046+868A>G
NM_015170.3:c.1377+868A>G NP_055985.2:n.1377+868A>G