Canonical Allele Identifier: CA1593661204

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344584A= , CM000667.2:g.156344584A=	GRCh38
NC_000005.9:g.155771594A= , CM000667.1:g.155771594A=	GRCh37
NC_000005.8:g.155704172A=	NCBI36
NG_008693.2:g.479241A= , LRG_205:g.479241A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.99A= MANE Select	ENSP00000338343.4:p.Arg33=
ENST00000337851.8:c.99A=	ENSP00000338343.4:p.Arg33=
ENST00000435422.7:c.96A=	ENSP00000403003.2:p.Arg32=
ENST00000517913.5:c.99A=	ENSP00000429378.1:p.Arg33=
ENST00000524347.2:c.99A=	ENSP00000430794.1:p.Arg33=
NM_000337.5:c.99A= , LRG_205t1:c.99A=	NP_000328.2:p.Arg33=
NM_001128209.1:c.96A=	NP_001121681.1:p.Arg32=
NM_172244.2:c.99A=	NP_758447.1:p.Arg33=
XM_005265966.3:c.99A=	XP_005266023.1:p.Arg33=
XM_005265967.1:c.99A=	XP_005266024.1:p.Arg33=
XM_006714911.2:c.99A=	XP_006714974.1:p.Arg33=
XM_011534621.1:c.96A=	XP_011532923.1:p.Arg32=
XR_941123.1:n.254+2869T=
XM_005265966.5:c.99A=	XP_005266023.1:p.Arg33=
XM_005265967.2:c.99A=	XP_005266024.1:p.Arg33=
XM_011534621.2:c.96A=	XP_011532923.1:p.Arg32=
XM_017009723.2:c.99A=	XP_016865212.1:p.Arg33=
XM_017009724.1:c.99A=	XP_016865213.1:p.Arg33=
NM_001128209.2:c.96A=	NP_001121681.1:p.Arg32=
NM_172244.3:c.99A=	NP_758447.1:p.Arg33=
NM_000337.6:c.99A= MANE Select	NP_000328.2:p.Arg33=