Canonical Allele Identifier: CA1766199791

Gene: SGCZ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15069730_15069731delinsCT , CM000670.2:g.15069730_15069731delinsCT	GRCh38
NC_000008.10:g.14927239_14927240delinsCT , CM000670.1:g.14927239_14927240delinsCT	GRCh37
NC_000008.9:g.14971610_14971611delinsCT	NCBI36
NG_008899.1:g.173553_173554delinsAG , LRG_208:g.173553_173554delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382080.6:c.39+167854_39+167855delinsAG MANE Select	ENSP00000371512.1:n.39+167854_39+167855delinsAG
ENST00000382080.5:c.39+167854_39+167855delinsAG	ENSP00000371512.1:n.39+167854_39+167855delinsAG
NM_139167.2:c.39+167854_39+167855delinsAG , LRG_208t1:c.39+167854_39+167855delinsAG	NP_631906.2:n.39+167854_39+167855delinsAG
NM_001322879.1:c.39+167854_39+167855delinsAG	NP_001309808.1:n.39+167854_39+167855delinsAG
NM_001322880.1:c.39+167854_39+167855delinsAG	NP_001309809.1:n.39+167854_39+167855delinsAG
NM_001322881.1:c.-90+167854_-90+167855delinsAG	NP_001309810.1:n.-90+167854_-90+167855delinsAG
NM_139167.3:c.39+167854_39+167855delinsAG	NP_631906.2:n.39+167854_39+167855delinsAG
NM_139167.4:c.39+167854_39+167855delinsAG MANE Select	NP_631906.2:n.39+167854_39+167855delinsAG
NM_001322879.2:c.39+167854_39+167855delinsAG	NP_001309808.1:n.39+167854_39+167855delinsAG
NM_001322880.2:c.39+167854_39+167855delinsAG	NP_001309809.1:n.39+167854_39+167855delinsAG
NM_001322881.2:c.-90+167854_-90+167855delinsAG	NP_001309810.1:n.-90+167854_-90+167855delinsAG