Canonical Allele Identifier: CA2676178449

Gene: SGCD

Linked Data

• gnomAD v4: 5-156594875-TTCTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156594886_156594891del , CM000667.2:g.156594886_156594891del	GRCh38
NC_000005.9:g.156021896_156021901del , CM000667.1:g.156021896_156021901del	GRCh37
NC_000005.8:g.155954474_155954479del	NCBI36
NG_008693.2:g.729543_729548del , LRG_205:g.729543_729548del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.383-46_383-41del MANE Select	ENSP00000338343.4:n.383-46_383-41del
ENST00000337851.8:c.383-46_383-41del	ENSP00000338343.4:n.383-46_383-41del
ENST00000435422.7:c.380-46_380-41del	ENSP00000403003.2:n.380-46_380-41del
ENST00000517913.5:c.383-46_383-41del	ENSP00000429378.1:n.383-46_383-41del
NM_000337.5:c.383-46_383-41del , LRG_205t1:c.383-46_383-41del	NP_000328.2:n.383-46_383-41del
NM_001128209.1:c.380-46_380-41del	NP_001121681.1:n.380-46_380-41del
NM_172244.2:c.383-46_383-41del	NP_758447.1:n.383-46_383-41del
XM_005265966.3:c.383-46_383-41del	XP_005266023.1:n.383-46_383-41del
XM_005265967.1:c.383-46_383-41del	XP_005266024.1:n.383-46_383-41del
XM_006714911.2:c.383-46_383-41del	XP_006714974.1:n.383-46_383-41del
XM_011534621.1:c.380-46_380-41del	XP_011532923.1:n.380-46_380-41del
XM_005265966.5:c.383-46_383-41del	XP_005266023.1:n.383-46_383-41del
XM_005265967.2:c.383-46_383-41del	XP_005266024.1:n.383-46_383-41del
XM_011534621.2:c.380-46_380-41del	XP_011532923.1:n.380-46_380-41del
XM_017009723.2:c.383-46_383-41del	XP_016865212.1:n.383-46_383-41del
XM_017009724.1:c.383-46_383-41del	XP_016865213.1:n.383-46_383-41del
NM_001128209.2:c.380-46_380-41del	NP_001121681.1:n.380-46_380-41del
NM_172244.3:c.383-46_383-41del	NP_758447.1:n.383-46_383-41del
NM_000337.6:c.383-46_383-41del MANE Select	NP_000328.2:n.383-46_383-41del