Canonical Allele Identifier: CA1593860638

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766934T= , CM000667.2:g.156766934T=	GRCh38
NC_000005.9:g.156193945T= , CM000667.1:g.156193945T=	GRCh37
NC_000005.8:g.156126523T=	NCBI36
NG_008693.2:g.901592T= , LRG_205:g.901592T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.*7544T= MANE Select	ENSP00000338343.4:n.*7544T=
ENST00000435422.7:c.*7544T=	ENSP00000403003.2:n.*7544T=
NM_000337.5:c.*7544T= , LRG_205t1:c.*7544T=	NP_000328.2:n.*7544T=
NM_001128209.1:c.*7544T=	NP_001121681.1:n.*7544T=
XM_005265966.3:c.*7544T=	XP_005266023.1:n.*7544T=
XM_006714911.2:c.*7544T=	XP_006714974.1:n.*7544T=
XM_011534621.1:c.*7544T=	XP_011532923.1:n.*7544T=
NM_001128209.2:c.*7544T=	NP_001121681.1:n.*7544T=
NM_000337.6:c.*7544T= MANE Select	NP_000328.2:n.*7544T=