Canonical Allele Identifier: CA447387924
Gene: SGCD HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.155935655A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508645A>C , CM000667.2:g.156508645A>C GRCh38
NC_000005.9:g.155935655A>C , CM000667.1:g.155935655A>C GRCh37
NC_000005.8:g.155868233A>C NCBI36
NG_008693.2:g.643302A>C , LRG_205:g.643302A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.237A>C MANE Select ENSP00000338343.4:p.Leu79=
ENST00000337851.8:c.237A>C ENSP00000338343.4:p.Leu79=
ENST00000435422.7:c.234A>C ENSP00000403003.2:p.Leu78=
ENST00000517913.5:c.237A>C ENSP00000429378.1:p.Leu79=
ENST00000524347.2:c.*101A>C ENSP00000430794.1:n.*101A>C
NM_000337.5:c.237A>C , LRG_205t1:c.237A>C NP_000328.2:p.Leu79=
NM_001128209.1:c.234A>C NP_001121681.1:p.Leu78=
NM_172244.2:c.237A>C NP_758447.1:p.Leu79=
XM_005265966.3:c.237A>C XP_005266023.1:p.Leu79=
XM_005265967.1:c.237A>C XP_005266024.1:p.Leu79=
XM_006714911.2:c.237A>C XP_006714974.1:p.Leu79=
XM_011534621.1:c.234A>C XP_011532923.1:p.Leu78=
XM_005265966.5:c.237A>C XP_005266023.1:p.Leu79=
XM_005265967.2:c.237A>C XP_005266024.1:p.Leu79=
XM_011534621.2:c.234A>C XP_011532923.1:p.Leu78=
XM_017009723.2:c.237A>C XP_016865212.1:p.Leu79=
XM_017009724.1:c.237A>C XP_016865213.1:p.Leu79=
NM_001128209.2:c.234A>C NP_001121681.1:p.Leu78=
NM_172244.3:c.237A>C NP_758447.1:p.Leu79=
NM_000337.6:c.237A>C MANE Select NP_000328.2:p.Leu79=
Search 100 bp 5'
Search 100 bp 3'