Canonical Allele Identifier: CA918207104
Gene: SGCZ HGNC NCBI

Linked Data

dbSNP Id: rs1563483353

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.15069491del , CM000670.2:g.15069491del GRCh38
NC_000008.10:g.14927000del , CM000670.1:g.14927000del GRCh37
NC_000008.9:g.14971371del NCBI36
NG_008899.1:g.173795del , LRG_208:g.173795del

Transcript Alleles

HGVS Amino-acid change
ENST00000382080.6:c.39+168096del MANE Select ENSP00000371512.1:n.39+168096del
ENST00000382080.5:c.39+168096del ENSP00000371512.1:n.39+168096del
NM_139167.2:c.39+168096del , LRG_208t1:c.39+168096del NP_631906.2:n.39+168096del
NM_001322879.1:c.39+168096del NP_001309808.1:n.39+168096del
NM_001322880.1:c.39+168096del NP_001309809.1:n.39+168096del
NM_001322881.1:c.-90+168096del NP_001309810.1:n.-90+168096del
NM_139167.3:c.39+168096del NP_631906.2:n.39+168096del
NM_139167.4:c.39+168096del MANE Select NP_631906.2:n.39+168096del
NM_001322879.2:c.39+168096del NP_001309808.1:n.39+168096del
NM_001322880.2:c.39+168096del NP_001309809.1:n.39+168096del
NM_001322881.2:c.-90+168096del NP_001309810.1:n.-90+168096del