Canonical Allele Identifier: CA1766199641
Gene: SGCZ HGNC NCBI

Linked Data

dbSNP Id: rs1646244224

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.15069500del , CM000670.2:g.15069500del GRCh38
NC_000008.10:g.14927009del , CM000670.1:g.14927009del GRCh37
NC_000008.9:g.14971380del NCBI36
NG_008899.1:g.173790del , LRG_208:g.173790del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382080.6:c.39+168091del MANE Select ENSP00000371512.1:n.39+168091del
ENST00000382080.5:c.39+168091del ENSP00000371512.1:n.39+168091del
NM_139167.2:c.39+168091del , LRG_208t1:c.39+168091del NP_631906.2:n.39+168091del
NM_001322879.1:c.39+168091del NP_001309808.1:n.39+168091del
NM_001322880.1:c.39+168091del NP_001309809.1:n.39+168091del
NM_001322881.1:c.-90+168091del NP_001309810.1:n.-90+168091del
NM_139167.3:c.39+168091del NP_631906.2:n.39+168091del
NM_139167.4:c.39+168091del MANE Select NP_631906.2:n.39+168091del
NM_001322879.2:c.39+168091del NP_001309808.1:n.39+168091del
NM_001322880.2:c.39+168091del NP_001309809.1:n.39+168091del
NM_001322881.2:c.-90+168091del NP_001309810.1:n.-90+168091del