Canonical Allele Identifier: CA2367229101

Gene: SULF2

Linked Data

• dbSNP Id: rs2087058618

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47661315_47661317del , CM000682.2:g.47661315_47661317del	GRCh38
NC_000020.10:g.46290059_46290061del , CM000682.1:g.46290059_46290061del	GRCh37
NC_000020.9:g.45723466_45723468del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698128.1:c.*2070+456_*2070+458del	ENSP00000513575.1:n.*2070+456_*2070+458del
ENST00000688720.1:c.2494+456_2494+458del MANE Select	ENSP00000508753.1:n.2494+456_2494+458del
ENST00000359930.8:c.2494+456_2494+458del	ENSP00000353007.4:n.2494+456_2494+458del
ENST00000467815.5:c.2494+456_2494+458del	ENSP00000418442.1:n.2494+456_2494+458del
ENST00000484875.5:c.2494+456_2494+458del	ENSP00000418290.1:n.2494+456_2494+458del
ENST00000495544.5:c.558+456_558+458del
NM_001161841.1:c.2494+456_2494+458del	NP_001155313.1:n.2494+456_2494+458del
NM_018837.3:c.2494+456_2494+458del	NP_061325.1:n.2494+456_2494+458del
NM_198596.2:c.2494+456_2494+458del	NP_940998.2:n.2494+456_2494+458del
XM_005260458.1:c.2494+456_2494+458del	XP_005260515.1:n.2494+456_2494+458del
XM_006723827.1:c.2497+456_2497+458del	XP_006723890.1:n.2497+456_2497+458del
XM_006723828.1:c.2497+456_2497+458del	XP_006723891.1:n.2497+456_2497+458del
XM_006723829.2:c.2497+456_2497+458del	XP_006723892.1:n.2497+456_2497+458del
XM_006723830.1:c.2494+456_2494+458del	XP_006723893.1:n.2494+456_2494+458del
XM_011528913.1:c.2497+456_2497+458del	XP_011527215.1:n.2497+456_2497+458del
XM_011528914.1:c.2497+456_2497+458del	XP_011527216.1:n.2497+456_2497+458del
XM_011528915.1:c.2497+456_2497+458del	XP_011527217.1:n.2497+456_2497+458del
XM_011528916.1:c.2494+456_2494+458del	XP_011527218.1:n.2494+456_2494+458del
XM_005260458.3:c.2494+456_2494+458del	XP_005260515.1:n.2494+456_2494+458del
XM_006723827.2:c.2497+456_2497+458del	XP_006723890.1:n.2497+456_2497+458del
XM_006723828.2:c.2497+456_2497+458del	XP_006723891.1:n.2497+456_2497+458del
XM_006723829.3:c.2497+456_2497+458del	XP_006723892.1:n.2497+456_2497+458del
XM_006723830.2:c.2494+456_2494+458del	XP_006723893.1:n.2494+456_2494+458del
XM_011528914.2:c.2497+456_2497+458del	XP_011527216.1:n.2497+456_2497+458del
XM_011528915.2:c.2497+456_2497+458del	XP_011527217.1:n.2497+456_2497+458del
XM_011528916.2:c.2494+456_2494+458del	XP_011527218.1:n.2494+456_2494+458del
XM_017027955.2:c.2494+456_2494+458del	XP_016883444.1:n.2494+456_2494+458del
NM_001161841.2:c.2494+456_2494+458del	NP_001155313.1:n.2494+456_2494+458del
NM_001387048.1:c.2494+456_2494+458del MANE Select	NP_001373977.1:n.2494+456_2494+458del
NM_001387049.1:c.2494+456_2494+458del	NP_001373978.1:n.2494+456_2494+458del
NM_001387050.1:c.2497+456_2497+458del	NP_001373979.1:n.2497+456_2497+458del
NM_001387051.1:c.2494+456_2494+458del	NP_001373980.1:n.2494+456_2494+458del
NM_001387052.1:c.2497+456_2497+458del	NP_001373981.1:n.2497+456_2497+458del
NM_001387053.1:c.2497+456_2497+458del	NP_001373982.1:n.2497+456_2497+458del
NM_001387054.1:c.2497+456_2497+458del	NP_001373983.1:n.2497+456_2497+458del
NM_001387055.1:c.2497+456_2497+458del	NP_001373984.1:n.2497+456_2497+458del
NM_018837.4:c.2494+456_2494+458del	NP_061325.1:n.2494+456_2494+458del
NM_198596.3:c.2494+456_2494+458del	NP_940998.2:n.2494+456_2494+458del