Canonical Allele Identifier: CA1593661347

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344900_156344912delinsCCTCCTTTAGAAT , CM000667.2:g.156344900_156344912delinsCCTCCTTTAGAAT	GRCh38
NC_000005.9:g.155771910_155771922delinsCCTCCTTTAGAAT , CM000667.1:g.155771910_155771922delinsCCTCCTTTAGAAT	GRCh37
NC_000005.8:g.155704488_155704500delinsCCTCCTTTAGAAT	NCBI36
NG_008693.2:g.479557_479569delinsCCTCCTTTAGAAT , LRG_205:g.479557_479569delinsCCTCCTTTAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.192+223_192+235delinsCCTCCTTTAGAAT MANE Select	ENSP00000338343.4:n.192+223_192+235delinsCCTCCTTTAGAAT
ENST00000337851.8:c.192+223_192+235delinsCCTCCTTTAGAAT	ENSP00000338343.4:n.192+223_192+235delinsCCTCCTTTAGAAT
ENST00000435422.7:c.189+223_189+235delinsCCTCCTTTAGAAT	ENSP00000403003.2:n.189+223_189+235delinsCCTCCTTTAGAAT
ENST00000517913.5:c.192+223_192+235delinsCCTCCTTTAGAAT	ENSP00000429378.1:n.192+223_192+235delinsCCTCCTTTAGAAT
ENST00000524347.2:c.192+223_192+235delinsCCTCCTTTAGAAT	ENSP00000430794.1:n.192+223_192+235delinsCCTCCTTTAGAAT
NM_000337.5:c.192+223_192+235delinsCCTCCTTTAGAAT , LRG_205t1:c.192+223_192+235delinsCCTCCTTTAGAAT	NP_000328.2:n.192+223_192+235delinsCCTCCTTTAGAAT
NM_001128209.1:c.189+223_189+235delinsCCTCCTTTAGAAT	NP_001121681.1:n.189+223_189+235delinsCCTCCTTTAGAAT
NM_172244.2:c.192+223_192+235delinsCCTCCTTTAGAAT	NP_758447.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_005265966.3:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_005266023.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_005265967.1:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_005266024.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_006714911.2:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_006714974.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_011534621.1:c.189+223_189+235delinsCCTCCTTTAGAAT	XP_011532923.1:n.189+223_189+235delinsCCTCCTTTAGAAT
XR_941123.1:n.254+2541_254+2553delinsATTCTAAAGGAGG
XM_005265966.5:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_005266023.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_005265967.2:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_005266024.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_011534621.2:c.189+223_189+235delinsCCTCCTTTAGAAT	XP_011532923.1:n.189+223_189+235delinsCCTCCTTTAGAAT
XM_017009723.2:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_016865212.1:n.192+223_192+235delinsCCTCCTTTAGAAT
XM_017009724.1:c.192+223_192+235delinsCCTCCTTTAGAAT	XP_016865213.1:n.192+223_192+235delinsCCTCCTTTAGAAT
NM_001128209.2:c.189+223_189+235delinsCCTCCTTTAGAAT	NP_001121681.1:n.189+223_189+235delinsCCTCCTTTAGAAT
NM_172244.3:c.192+223_192+235delinsCCTCCTTTAGAAT	NP_758447.1:n.192+223_192+235delinsCCTCCTTTAGAAT
NM_000337.6:c.192+223_192+235delinsCCTCCTTTAGAAT MANE Select	NP_000328.2:n.192+223_192+235delinsCCTCCTTTAGAAT