Canonical Allele Identifier: CA1593860652

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766950A= , CM000667.2:g.156766950A=	GRCh38
NC_000005.9:g.156193961A= , CM000667.1:g.156193961A=	GRCh37
NC_000005.8:g.156126539A=	NCBI36
NG_008693.2:g.901608A= , LRG_205:g.901608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.*7560A= MANE Select	ENSP00000338343.4:n.*7560A=
ENST00000435422.7:c.*7560A=	ENSP00000403003.2:n.*7560A=
NM_000337.5:c.*7560A= , LRG_205t1:c.*7560A=	NP_000328.2:n.*7560A=
NM_001128209.1:c.*7560A=	NP_001121681.1:n.*7560A=
XM_005265966.3:c.*7560A=	XP_005266023.1:n.*7560A=
XM_006714911.2:c.*7560A=	XP_006714974.1:n.*7560A=
XM_011534621.1:c.*7560A=	XP_011532923.1:n.*7560A=
NM_001128209.2:c.*7560A=	NP_001121681.1:n.*7560A=
NM_000337.6:c.*7560A= MANE Select	NP_000328.2:n.*7560A=