Canonical Allele Identifier: CA1766199639

Gene: SGCZ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15069488_15069489delinsCT , CM000670.2:g.15069488_15069489delinsCT	GRCh38
NC_000008.10:g.14926997_14926998delinsCT , CM000670.1:g.14926997_14926998delinsCT	GRCh37
NC_000008.9:g.14971368_14971369delinsCT	NCBI36
NG_008899.1:g.173795_173796delinsAG , LRG_208:g.173795_173796delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382080.6:c.39+168096_39+168097delinsAG MANE Select	ENSP00000371512.1:n.39+168096_39+168097delinsAG
ENST00000382080.5:c.39+168096_39+168097delinsAG	ENSP00000371512.1:n.39+168096_39+168097delinsAG
NM_139167.2:c.39+168096_39+168097delinsAG , LRG_208t1:c.39+168096_39+168097delinsAG	NP_631906.2:n.39+168096_39+168097delinsAG
NM_001322879.1:c.39+168096_39+168097delinsAG	NP_001309808.1:n.39+168096_39+168097delinsAG
NM_001322880.1:c.39+168096_39+168097delinsAG	NP_001309809.1:n.39+168096_39+168097delinsAG
NM_001322881.1:c.-90+168096_-90+168097delinsAG	NP_001309810.1:n.-90+168096_-90+168097delinsAG
NM_139167.3:c.39+168096_39+168097delinsAG	NP_631906.2:n.39+168096_39+168097delinsAG
NM_139167.4:c.39+168096_39+168097delinsAG MANE Select	NP_631906.2:n.39+168096_39+168097delinsAG
NM_001322879.2:c.39+168096_39+168097delinsAG	NP_001309808.1:n.39+168096_39+168097delinsAG
NM_001322880.2:c.39+168096_39+168097delinsAG	NP_001309809.1:n.39+168096_39+168097delinsAG
NM_001322881.2:c.-90+168096_-90+168097delinsAG	NP_001309810.1:n.-90+168096_-90+168097delinsAG