Canonical Allele Identifier: CA172674951

Gene: SGCZ

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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