Canonical Allele Identifier: CA1765911960
Community Standard Title: NM_139167.4(SGCZ):c.40-53246G=
Gene: SGCZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.14608172C= , CM000670.2:g.14608172C= GRCh38
NC_000008.10:g.14465681C= , CM000670.1:g.14465681C= GRCh37
NC_000008.9:g.14510052C= NCBI36
NG_008899.1:g.635112G= , LRG_208:g.635112G=

Transcript Alleles

HGVS Amino-acid Change
NM_139167.4:c.40-53246G= MANE Select NP_631906.2:n.40-53246G=
ENST00000382080.6:c.40-53246G= MANE Select ENSP00000371512.1:n.40-53246G=
NM_001322879.1:c.40-53246G= NP_001309808.1:n.40-53246G=
NM_001322879.2:c.40-53246G= NP_001309808.1:n.40-53246G=
NM_001322880.1:c.40-53246G= NP_001309809.1:n.40-53246G=
NM_001322880.2:c.40-53246G= NP_001309809.1:n.40-53246G=
NM_001322881.1:c.-89-53246G= NP_001309810.1:n.-89-53246G=
NM_001322881.2:c.-89-53246G= NP_001309810.1:n.-89-53246G=
NM_139167.2:c.40-53246G= , LRG_208t1:c.40-53246G= NP_631906.2:n.40-53246G=
NM_139167.3:c.40-53246G= NP_631906.2:n.40-53246G=
ENST00000382080.5:c.40-53246G= ENSP00000371512.1:n.40-53246G=