Canonical Allele Identifier: CA8817836

Linked Data

ClinVar Variation Id: 642734
ClinVar RCV Id: RCV000796248
dbSNP Id: rs374621913

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80213852G>C , CM000679.2:g.80213852G>C GRCh38
NC_000017.10:g.78187651G>C , CM000679.1:g.78187651G>C GRCh37
NC_000017.9:g.75802246G>C NCBI36
NG_008229.1:g.11549C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703570.1:n.2845-2014G>C (CARD14)
ENST00000326317.11:c.697C>G (SGSH) MANE Select ENSP00000314606.6:p.Arg233Gly
ENST00000326317.10:c.697C>G (SGSH) ENSP00000314606.6:p.Arg233Gly
ENST00000570923.1:c.732C>G (SGSH) ENSP00000458200.1:p.Pro244=
ENST00000572208.5:n.564C>G (SGSH)
ENST00000572257.5:c.299C>G (SGSH)
ENST00000573150.5:c.591C>G (SGSH) ENSP00000459280.1:p.Pro197=
ENST00000574505.5:c.556C>G (SGSH)
ENST00000575282.5:n.992C>G (SGSH)
ENST00000576941.5:c.*113C>G (SGSH) ENSP00000461160.1:n.*113C>G
NM_000199.3:c.697C>G (SGSH) NP_000190.1:p.Arg233Gly
XM_005257582.2:c.697C>G (SGSH) XP_005257639.1:p.Arg233Gly
XM_005257583.3:c.697C>G (SGSH) XP_005257640.1:p.Arg233Gly
XM_011525126.1:c.697C>G (SGSH) XP_011523428.1:p.Arg233Gly
XM_011525127.1:c.697C>G (SGSH) XP_011523429.1:p.Arg233Gly
XR_934532.1:n.717C>G (SGSH)
NM_000199.4:c.697C>G (SGSH) NP_000190.1:p.Arg233Gly
NM_001352921.1:c.697C>G (SGSH) NP_001339850.1:p.Arg233Gly
NM_001352922.1:c.697C>G (SGSH) NP_001339851.1:p.Arg233Gly
NR_148201.1:n.678C>G (SGSH)
XM_005257583.4:c.697C>G (SGSH) XP_005257640.1:p.Arg233Gly
XM_017024952.1:c.697C>G (SGSH) XP_016880441.1:p.Arg233Gly
XR_001752585.1:n.717C>G (SGSH)
XR_001752586.1:n.717C>G (SGSH)
XR_001752587.1:n.717C>G (SGSH)
XR_001752588.1:n.717C>G (SGSH)
XR_001752589.1:n.717C>G (SGSH)
XR_001752590.1:n.717C>G (SGSH)
XR_001752591.1:n.717C>G (SGSH)
XR_001752592.1:n.717C>G (SGSH)
XR_002958057.1:n.717C>G (SGSH)
XR_934532.2:n.717C>G (SGSH)
NM_000199.5:c.697C>G (SGSH) MANE Select NP_000190.1:p.Arg233Gly
NM_001352921.2:c.697C>G (SGSH) NP_001339850.1:p.Arg233Gly
NM_001352922.2:c.697C>G (SGSH) NP_001339851.1:p.Arg233Gly
NR_148201.2:n.611C>G (SGSH)
NM_001352921.3:c.697C>G (SGSH) NP_001339850.1:p.Arg233Gly