Canonical Allele Identifier: CA1765685552

Gene: SGCZ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.14256307G= , CM000670.2:g.14256307G=	GRCh38
NC_000008.10:g.14113816G= , CM000670.1:g.14113816G=	GRCh37
NC_000008.9:g.14158187G=	NCBI36
NG_008899.1:g.986977C= , LRG_208:g.986977C=

Transcript Alleles

HGVS	Amino-acid Change
NM_139167.4:c.337-18628C= MANE Select	NP_631906.2:n.337-18628C=
ENST00000382080.6:c.337-18628C= MANE Select	ENSP00000371512.1:n.337-18628C=
NM_001322879.1:c.235-18628C=	NP_001309808.1:n.235-18628C=
NM_001322879.2:c.235-18628C=	NP_001309808.1:n.235-18628C=
NM_001322880.1:c.337-18628C=	NP_001309809.1:n.337-18628C=
NM_001322880.2:c.337-18628C=	NP_001309809.1:n.337-18628C=
NM_001322881.1:c.115-18628C=	NP_001309810.1:n.115-18628C=
NM_001322881.2:c.115-18628C=	NP_001309810.1:n.115-18628C=
NM_139167.2:c.337-18628C= , LRG_208t1:c.337-18628C=	NP_631906.2:n.337-18628C=
NM_139167.3:c.337-18628C=	NP_631906.2:n.337-18628C=
ENST00000382080.5:c.337-18628C=	ENSP00000371512.1:n.337-18628C=
ENST00000421524.6:c.196-18628C=	ENSP00000405224.2:n.196-18628C=
ENST00000613692.1:c.-57-18628C=	ENSP00000481839.1:n.-57-18628C=