Canonical Allele Identifier: CA401362892

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80214698C>A , CM000679.2:g.80214698C>A GRCh38
NC_000017.10:g.78188497C>A , CM000679.1:g.78188497C>A GRCh37
NC_000017.9:g.75803092C>A NCBI36
NG_008229.1:g.10703G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703570.1:n.2845-1168C>A (CARD14)
ENST00000326317.11:c.423G>T (SGSH) MANE Select ENSP00000314606.6:p.Glu141Asp
ENST00000326317.10:c.423G>T (SGSH) ENSP00000314606.6:p.Glu141Asp
ENST00000570427.1:c.441G>T (SGSH) ENSP00000459765.1:p.Glu147Asp
ENST00000570923.1:c.458G>T (SGSH) ENSP00000458200.1:p.Arg153Ile
ENST00000571051.5:n.375+335G>T (SGSH)
ENST00000571675.5:n.443G>T (SGSH)
ENST00000572208.5:n.373+335G>T (SGSH)
ENST00000572257.5:c.25G>T (SGSH)
ENST00000573150.5:c.317G>T (SGSH) ENSP00000459280.1:p.Arg106Ile
ENST00000574505.5:c.301-19G>T (SGSH)
ENST00000575282.5:n.432G>T (SGSH)
ENST00000576707.5:c.162G>T (SGSH) ENSP00000461128.1:p.Glu54Asp
ENST00000576941.5:c.250-370G>T (SGSH) ENSP00000461160.1:n.250-370G>T
NM_000199.3:c.423G>T (SGSH) NP_000190.1:p.Glu141Asp
XM_005257582.2:c.423G>T (SGSH) XP_005257639.1:p.Glu141Asp
XM_005257583.3:c.423G>T (SGSH) XP_005257640.1:p.Glu141Asp
XM_011525126.1:c.423G>T (SGSH) XP_011523428.1:p.Glu141Asp
XM_011525127.1:c.423G>T (SGSH) XP_011523429.1:p.Glu141Asp
XR_934532.1:n.443G>T (SGSH)
NM_000199.4:c.423G>T (SGSH) NP_000190.1:p.Glu141Asp
NM_001352921.1:c.423G>T (SGSH) NP_001339850.1:p.Glu141Asp
NM_001352922.1:c.423G>T (SGSH) NP_001339851.1:p.Glu141Asp
NR_148201.1:n.404G>T (SGSH)
XM_005257583.4:c.423G>T (SGSH) XP_005257640.1:p.Glu141Asp
XM_017024952.1:c.423G>T (SGSH) XP_016880441.1:p.Glu141Asp
XR_001752585.1:n.443G>T (SGSH)
XR_001752586.1:n.443G>T (SGSH)
XR_001752587.1:n.443G>T (SGSH)
XR_001752588.1:n.443G>T (SGSH)
XR_001752589.1:n.443G>T (SGSH)
XR_001752590.1:n.443G>T (SGSH)
XR_001752591.1:n.443G>T (SGSH)
XR_001752592.1:n.443G>T (SGSH)
XR_002958057.1:n.443G>T (SGSH)
XR_934532.2:n.443G>T (SGSH)
NM_000199.5:c.423G>T (SGSH) MANE Select NP_000190.1:p.Glu141Asp
NM_001352921.2:c.423G>T (SGSH) NP_001339850.1:p.Glu141Asp
NM_001352922.2:c.423G>T (SGSH) NP_001339851.1:p.Glu141Asp
NR_148201.2:n.337G>T (SGSH)
NM_001352921.3:c.423G>T (SGSH) NP_001339850.1:p.Glu141Asp