Canonical Allele Identifier: CA362010146

Gene: SGCD

Linked Data

• MyVariant Identifiers: chr5:g.156594906del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156594906del , CM000667.2:g.156594906del	GRCh38
NC_000005.9:g.156021916del , CM000667.1:g.156021916del	GRCh37
NC_000005.8:g.155954494del	NCBI36
NG_008693.2:g.729563del , LRG_205:g.729563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.383-26del MANE Select	ENSP00000338343.4:n.383-26del
ENST00000337851.8:c.383-26del	ENSP00000338343.4:n.383-26del
ENST00000435422.7:c.380-26del	ENSP00000403003.2:n.380-26del
ENST00000517913.5:c.383-26del	ENSP00000429378.1:n.383-26del
NM_000337.5:c.383-26del , LRG_205t1:c.383-26del	NP_000328.2:n.383-26del
NM_001128209.1:c.380-26del	NP_001121681.1:n.380-26del
NM_172244.2:c.383-26del	NP_758447.1:n.383-26del
XM_005265966.3:c.383-26del	XP_005266023.1:n.383-26del
XM_005265967.1:c.383-26del	XP_005266024.1:n.383-26del
XM_006714911.2:c.383-26del	XP_006714974.1:n.383-26del
XM_011534621.1:c.380-26del	XP_011532923.1:n.380-26del
XM_005265966.5:c.383-26del	XP_005266023.1:n.383-26del
XM_005265967.2:c.383-26del	XP_005266024.1:n.383-26del
XM_011534621.2:c.380-26del	XP_011532923.1:n.380-26del
XM_017009723.2:c.383-26del	XP_016865212.1:n.383-26del
XM_017009724.1:c.383-26del	XP_016865213.1:n.383-26del
NM_001128209.2:c.380-26del	NP_001121681.1:n.380-26del
NM_172244.3:c.383-26del	NP_758447.1:n.383-26del
NM_000337.6:c.383-26del MANE Select	NP_000328.2:n.383-26del