Canonical Allele Identifier: CA12936740

Gene: SGCZ

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.14316465G>T , CM000670.2:g.14316465G>T	GRCh38
NC_000008.10:g.14173974G>T , CM000670.1:g.14173974G>T	GRCh37
NC_000008.9:g.14218345G>T	NCBI36
NG_008899.1:g.926819C>A , LRG_208:g.926819C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382080.6:c.336+7638C>A MANE Select	ENSP00000371512.1:n.336+7638C>A
ENST00000382080.5:c.336+7638C>A	ENSP00000371512.1:n.336+7638C>A
ENST00000421524.6:c.196-78786C>A	ENSP00000405224.2:n.196-78786C>A
ENST00000613692.1:c.-58+7638C>A	ENSP00000481839.1:n.-58+7638C>A
NM_139167.2:c.336+7638C>A , LRG_208t1:c.336+7638C>A	NP_631906.2:n.336+7638C>A
NM_001322879.1:c.235-78786C>A	NP_001309808.1:n.235-78786C>A
NM_001322880.1:c.336+7638C>A	NP_001309809.1:n.336+7638C>A
NM_001322881.1:c.114+7638C>A	NP_001309810.1:n.114+7638C>A
NM_139167.3:c.336+7638C>A	NP_631906.2:n.336+7638C>A
NM_139167.4:c.336+7638C>A MANE Select	NP_631906.2:n.336+7638C>A
NM_001322879.2:c.235-78786C>A	NP_001309808.1:n.235-78786C>A
NM_001322880.2:c.336+7638C>A	NP_001309809.1:n.336+7638C>A
NM_001322881.2:c.114+7638C>A	NP_001309810.1:n.114+7638C>A