Canonical Allele Identifier: CA1593779133

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156594970G= , CM000667.2:g.156594970G=	GRCh38
NC_000005.9:g.156021980G= , CM000667.1:g.156021980G=	GRCh37
NC_000005.8:g.155954558G=	NCBI36
NG_008693.2:g.729627G= , LRG_205:g.729627G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.421G= MANE Select	ENSP00000338343.4:p.Val141=
ENST00000337851.8:c.421G=	ENSP00000338343.4:p.Val141=
ENST00000435422.7:c.418G=	ENSP00000403003.2:p.Val140=
ENST00000517913.5:c.421G=	ENSP00000429378.1:p.Val141=
NM_000337.5:c.421G= , LRG_205t1:c.421G=	NP_000328.2:p.Val141=
NM_001128209.1:c.418G=	NP_001121681.1:p.Val140=
NM_172244.2:c.421G=	NP_758447.1:p.Val141=
XM_005265966.3:c.421G=	XP_005266023.1:p.Val141=
XM_005265967.1:c.421G=	XP_005266024.1:p.Val141=
XM_006714911.2:c.421G=	XP_006714974.1:p.Val141=
XM_011534621.1:c.418G=	XP_011532923.1:p.Val140=
XM_005265966.5:c.421G=	XP_005266023.1:p.Val141=
XM_005265967.2:c.421G=	XP_005266024.1:p.Val141=
XM_011534621.2:c.418G=	XP_011532923.1:p.Val140=
XM_017009723.2:c.421G=	XP_016865212.1:p.Val141=
XM_017009724.1:c.421G=	XP_016865213.1:p.Val141=
NM_001128209.2:c.418G=	NP_001121681.1:p.Val140=
NM_172244.3:c.421G=	NP_758447.1:p.Val141=
NM_000337.6:c.421G= MANE Select	NP_000328.2:p.Val141=