Canonical Allele Identifier: CA362007644
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156344559T>A , CM000667.2:g.156344559T>A GRCh38
NC_000005.9:g.155771569T>A , CM000667.1:g.155771569T>A GRCh37
NC_000005.8:g.155704147T>A NCBI36
NG_008693.2:g.479216T>A , LRG_205:g.479216T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.74T>A MANE Select ENSP00000338343.4:p.Val25Glu
ENST00000337851.8:c.74T>A ENSP00000338343.4:p.Val25Glu
ENST00000435422.7:c.71T>A ENSP00000403003.2:p.Val24Glu
ENST00000517913.5:c.74T>A ENSP00000429378.1:p.Val25Glu
ENST00000524347.2:c.74T>A ENSP00000430794.1:p.Val25Glu
NM_000337.5:c.74T>A , LRG_205t1:c.74T>A NP_000328.2:p.Val25Glu
NM_001128209.1:c.71T>A NP_001121681.1:p.Val24Glu
NM_172244.2:c.74T>A NP_758447.1:p.Val25Glu
XM_005265966.3:c.74T>A XP_005266023.1:p.Val25Glu
XM_005265967.1:c.74T>A XP_005266024.1:p.Val25Glu
XM_006714911.2:c.74T>A XP_006714974.1:p.Val25Glu
XM_011534621.1:c.71T>A XP_011532923.1:p.Val24Glu
XR_941123.1:n.254+2894A>T
XM_005265966.5:c.74T>A XP_005266023.1:p.Val25Glu
XM_005265967.2:c.74T>A XP_005266024.1:p.Val25Glu
XM_011534621.2:c.71T>A XP_011532923.1:p.Val24Glu
XM_017009723.2:c.74T>A XP_016865212.1:p.Val25Glu
XM_017009724.1:c.74T>A XP_016865213.1:p.Val25Glu
NM_001128209.2:c.71T>A NP_001121681.1:p.Val24Glu
NM_172244.3:c.74T>A NP_758447.1:p.Val25Glu
NM_000337.6:c.74T>A MANE Select NP_000328.2:p.Val25Glu