Canonical Allele Identifier: CA1593738850
Gene: SGCD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508679G= , CM000667.2:g.156508679G= GRCh38
NC_000005.9:g.155935689G= , CM000667.1:g.155935689G= GRCh37
NC_000005.8:g.155868267G= NCBI36
NG_008693.2:g.643336G= , LRG_205:g.643336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.271G= MANE Select ENSP00000338343.4:p.Ala91=
ENST00000337851.8:c.271G= ENSP00000338343.4:p.Ala91=
ENST00000435422.7:c.268G= ENSP00000403003.2:p.Ala90=
ENST00000517913.5:c.271G= ENSP00000429378.1:p.Ala91=
ENST00000524347.2:c.*135G= ENSP00000430794.1:n.*135G=
NM_000337.5:c.271G= , LRG_205t1:c.271G= NP_000328.2:p.Ala91=
NM_001128209.1:c.268G= NP_001121681.1:p.Ala90=
NM_172244.2:c.271G= NP_758447.1:p.Ala91=
XM_005265966.3:c.271G= XP_005266023.1:p.Ala91=
XM_005265967.1:c.271G= XP_005266024.1:p.Ala91=
XM_006714911.2:c.271G= XP_006714974.1:p.Ala91=
XM_011534621.1:c.268G= XP_011532923.1:p.Ala90=
XM_005265966.5:c.271G= XP_005266023.1:p.Ala91=
XM_005265967.2:c.271G= XP_005266024.1:p.Ala91=
XM_011534621.2:c.268G= XP_011532923.1:p.Ala90=
XM_017009723.2:c.271G= XP_016865212.1:p.Ala91=
XM_017009724.1:c.271G= XP_016865213.1:p.Ala91=
NM_001128209.2:c.268G= NP_001121681.1:p.Ala90=
NM_172244.3:c.271G= NP_758447.1:p.Ala91=
NM_000337.6:c.271G= MANE Select NP_000328.2:p.Ala91=
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