Canonical Allele Identifier: CA1593661098

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344411_156344412delinsAT , CM000667.2:g.156344411_156344412delinsAT	GRCh38
NC_000005.9:g.155771421_155771422delinsAT , CM000667.1:g.155771421_155771422delinsAT	GRCh37
NC_000005.8:g.155703999_155704000delinsAT	NCBI36
NG_008693.2:g.479068_479069delinsAT , LRG_205:g.479068_479069delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.4-78_4-77delinsAT MANE Select	ENSP00000338343.4:n.4-78_4-77delinsAT
ENST00000337851.8:c.4-78_4-77delinsAT	ENSP00000338343.4:n.4-78_4-77delinsAT
ENST00000435422.7:c.1-78_1-77delinsAT	ENSP00000403003.2:n.1-78_1-77delinsAT
ENST00000517913.5:c.4-78_4-77delinsAT	ENSP00000429378.1:n.4-78_4-77delinsAT
ENST00000524347.2:c.4-78_4-77delinsAT	ENSP00000430794.1:n.4-78_4-77delinsAT
NM_000337.5:c.4-78_4-77delinsAT , LRG_205t1:c.4-78_4-77delinsAT	NP_000328.2:n.4-78_4-77delinsAT
NM_001128209.1:c.1-78_1-77delinsAT	NP_001121681.1:n.1-78_1-77delinsAT
NM_172244.2:c.4-78_4-77delinsAT	NP_758447.1:n.4-78_4-77delinsAT
XM_005265966.3:c.4-78_4-77delinsAT	XP_005266023.1:n.4-78_4-77delinsAT
XM_005265967.1:c.4-78_4-77delinsAT	XP_005266024.1:n.4-78_4-77delinsAT
XM_006714911.2:c.4-78_4-77delinsAT	XP_006714974.1:n.4-78_4-77delinsAT
XM_011534621.1:c.1-78_1-77delinsAT	XP_011532923.1:n.1-78_1-77delinsAT
XR_941123.1:n.254+3041_254+3042delinsAT
XM_005265966.5:c.4-78_4-77delinsAT	XP_005266023.1:n.4-78_4-77delinsAT
XM_005265967.2:c.4-78_4-77delinsAT	XP_005266024.1:n.4-78_4-77delinsAT
XM_011534621.2:c.1-78_1-77delinsAT	XP_011532923.1:n.1-78_1-77delinsAT
XM_017009723.2:c.4-78_4-77delinsAT	XP_016865212.1:n.4-78_4-77delinsAT
XM_017009724.1:c.4-78_4-77delinsAT	XP_016865213.1:n.4-78_4-77delinsAT
NM_001128209.2:c.1-78_1-77delinsAT	NP_001121681.1:n.1-78_1-77delinsAT
NM_172244.3:c.4-78_4-77delinsAT	NP_758447.1:n.4-78_4-77delinsAT
NM_000337.6:c.4-78_4-77delinsAT MANE Select	NP_000328.2:n.4-78_4-77delinsAT