Canonical Allele Identifier: CA2579571585
Gene: SMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.21978953del , CM000685.2:g.21978953del GRCh38
NC_000023.10:g.21997071del , CM000685.1:g.21997071del GRCh37
NC_000023.9:g.21906992del NCBI36
NG_009228.1:g.43230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404933.7:c.737del MANE Select ENSP00000385746.2:p.Gly246GlufsTer7
ENST00000379404.5:c.578del ENSP00000368714.1:p.Gly193GlufsTer7
ENST00000404933.6:c.737del ENSP00000385746.2:p.Gly246GlufsTer7
NM_001258423.1:c.578del NP_001245352.1:p.Gly193GlufsTer7
NM_004595.4:c.737del NP_004586.2:p.Gly246GlufsTer7
XM_005274582.1:c.635del XP_005274639.1:p.Gly212GlufsTer7
XM_011545568.1:c.635del XP_011543870.1:p.Gly212GlufsTer7
XM_005274582.2:c.635del XP_005274639.1:p.Gly212GlufsTer7
XM_011545568.2:c.635del XP_011543870.1:p.Gly212GlufsTer7
XM_017029753.2:c.737del XP_016885242.1:p.Gly246GlufsTer7
XM_017029754.1:c.635del XP_016885243.1:p.Gly212GlufsTer7
XM_017029755.1:c.635del XP_016885244.1:p.Gly212GlufsTer7
XM_024452427.1:c.635del XP_024308195.1:p.Gly212GlufsTer7
NM_004595.5:c.737del MANE Select NP_004586.2:p.Gly246GlufsTer7
NM_001258423.2:c.578del NP_001245352.1:p.Gly193GlufsTer7