Canonical Allele Identifier: CA14789273

Gene: SULF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47771969T>C , CM000682.2:g.47771969T>C	GRCh38
NC_000020.10:g.46400713T>C , CM000682.1:g.46400713T>C	GRCh37
NC_000020.9:g.45834120T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698128.1:c.-101+14079A>G	ENSP00000513575.1:n.-101+14079A>G
ENST00000688720.1:c.-101+13374A>G MANE Select	ENSP00000508753.1:n.-101+13374A>G
ENST00000359930.8:c.-101+13866A>G	ENSP00000353007.4:n.-101+13866A>G
ENST00000437955.1:c.-101+13374A>G	ENSP00000410026.1:n.-101+13374A>G
ENST00000463221.2:n.220+13866A>G
ENST00000467815.5:c.-101+14079A>G	ENSP00000418442.1:n.-101+14079A>G
ENST00000484875.5:c.-101+14079A>G	ENSP00000418290.1:n.-101+14079A>G
NM_001161841.1:c.-101+14079A>G	NP_001155313.1:n.-101+14079A>G
NM_018837.3:c.-101+13866A>G	NP_061325.1:n.-101+13866A>G
NM_198596.2:c.-101+14079A>G	NP_940998.2:n.-101+14079A>G
XM_005260458.1:c.-101+13374A>G	XP_005260515.1:n.-101+13374A>G
XM_006723827.1:c.-101+13374A>G	XP_006723890.1:n.-101+13374A>G
XM_006723828.1:c.-101+14079A>G	XP_006723891.1:n.-101+14079A>G
XM_006723829.2:c.-101+13866A>G	XP_006723892.1:n.-101+13866A>G
XM_006723830.1:c.-101+13374A>G	XP_006723893.1:n.-101+13374A>G
XM_011528914.1:c.-101+13374A>G	XP_011527216.1:n.-101+13374A>G
XM_011528915.1:c.-101+13374A>G	XP_011527217.1:n.-101+13374A>G
XM_011528916.1:c.-101+14079A>G	XP_011527218.1:n.-101+14079A>G
XM_005260458.3:c.-101+13374A>G	XP_005260515.1:n.-101+13374A>G
XM_006723827.2:c.-101+13374A>G	XP_006723890.1:n.-101+13374A>G
XM_006723828.2:c.-101+14079A>G	XP_006723891.1:n.-101+14079A>G
XM_006723829.3:c.-101+13866A>G	XP_006723892.1:n.-101+13866A>G
XM_006723830.2:c.-101+13374A>G	XP_006723893.1:n.-101+13374A>G
XM_011528914.2:c.-101+13374A>G	XP_011527216.1:n.-101+13374A>G
XM_011528915.2:c.-101+13374A>G	XP_011527217.1:n.-101+13374A>G
XM_011528916.2:c.-101+14079A>G	XP_011527218.1:n.-101+14079A>G
NM_001161841.2:c.-101+14079A>G	NP_001155313.1:n.-101+14079A>G
NM_001387048.1:c.-101+13374A>G MANE Select	NP_001373977.1:n.-101+13374A>G
NM_001387050.1:c.-101+13374A>G	NP_001373979.1:n.-101+13374A>G
NM_001387051.1:c.-101+14079A>G	NP_001373980.1:n.-101+14079A>G
NM_001387052.1:c.-101+14079A>G	NP_001373981.1:n.-101+14079A>G
NM_001387053.1:c.-101+13866A>G	NP_001373982.1:n.-101+13866A>G
NM_001387054.1:c.-101+13374A>G	NP_001373983.1:n.-101+13374A>G
NM_018837.4:c.-101+13866A>G	NP_061325.1:n.-101+13866A>G
NM_198596.3:c.-101+14079A>G	NP_940998.2:n.-101+14079A>G