Canonical Allele Identifier: CA1593642162

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156329461G= , CM000667.2:g.156329461G=	GRCh38
NC_000005.9:g.155756471G= , CM000667.1:g.155756471G=	GRCh37
NC_000005.8:g.155689049G=	NCBI36
NG_008693.2:g.464118G= , LRG_205:g.464118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.-43-73G= MANE Select	ENSP00000338343.4:n.-43-73G=
ENST00000337851.8:c.-43-73G=	ENSP00000338343.4:n.-43-73G=
ENST00000435422.7:c.-1+2229G=	ENSP00000403003.2:n.-1+2229G=
ENST00000517913.5:c.-43-73G=	ENSP00000429378.1:n.-43-73G=
ENST00000524347.2:c.-43-73G=	ENSP00000430794.1:n.-43-73G=
NM_000337.5:c.-43-73G= , LRG_205t1:c.-43-73G=	NP_000328.2:n.-43-73G=
NM_001128209.1:c.-1+2229G=	NP_001121681.1:n.-1+2229G=
NM_172244.2:c.-43-73G=	NP_758447.1:n.-43-73G=
XM_005265966.3:c.-43-73G=	XP_005266023.1:n.-43-73G=
XM_005265967.1:c.-43-73G=	XP_005266024.1:n.-43-73G=
XM_006714911.2:c.-43-73G=	XP_006714974.1:n.-43-73G=
XM_011534621.1:c.1-15028G=	XP_011532923.1:n.1-15028G=
XR_941123.1:n.254+17992C=
XM_005265966.5:c.-43-73G=	XP_005266023.1:n.-43-73G=
XM_005265967.2:c.-43-73G=	XP_005266024.1:n.-43-73G=
XM_011534621.2:c.1-15028G=	XP_011532923.1:n.1-15028G=
XM_017009723.2:c.-43-73G=	XP_016865212.1:n.-43-73G=
XM_017009724.1:c.-43-73G=	XP_016865213.1:n.-43-73G=
NM_001128209.2:c.-1+2229G=	NP_001121681.1:n.-1+2229G=
NM_172244.3:c.-43-73G=	NP_758447.1:n.-43-73G=
NM_000337.6:c.-43-73G= MANE Select	NP_000328.2:n.-43-73G=