Canonical Allele Identifier: CA175884098

Gene: GOLGA7

Linked Data

• dbSNP Id: rs572701217
• gnomAD v2: 8-41368222-G-A
• gnomAD v3: 8-41510703-G-A
• gnomAD v4: 8-41510703-G-A
• MyVariant Identifiers: chr8:g.41368222G>A (hg19) ; chr8:g.41510703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41510703G>A , CM000670.2:g.41510703G>A	GRCh38
NC_000008.10:g.41368222G>A , CM000670.1:g.41368222G>A	GRCh37
NC_000008.9:g.41487379G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405786.3:c.*1149G>A	ENSP00000386030.2:n.*1149G>A
ENST00000518270.6:c.*1135G>A	ENSP00000429329.1:n.*1135G>A
ENST00000694863.1:c.*1135G>A	ENSP00000511547.1:n.*1135G>A
ENST00000694872.1:c.*1135G>A	ENSP00000511557.1:n.*1135G>A
ENST00000694873.1:c.*1135G>A	ENSP00000511558.1:n.*1135G>A
ENST00000694874.1:c.*1135G>A	ENSP00000511559.1:n.*1135G>A
ENST00000694875.1:c.*1135G>A	ENSP00000511560.1:n.*1135G>A
ENST00000694876.1:c.*985G>A	ENSP00000511561.1:n.*985G>A
ENST00000694877.1:c.*1149G>A	ENSP00000511562.1:n.*1149G>A
ENST00000694878.1:c.*1149G>A	ENSP00000511563.1:n.*1149G>A
ENST00000694879.1:n.1406G>A
ENST00000694883.1:c.*1149G>A	ENSP00000511567.1:n.*1149G>A
ENST00000694884.1:c.*1209G>A	ENSP00000511568.1:n.*1209G>A
ENST00000694885.1:n.2656G>A
ENST00000694886.1:c.*1135G>A	ENSP00000511569.1:n.*1135G>A
ENST00000694887.1:c.*1135G>A	ENSP00000511570.1:n.*1135G>A
ENST00000694888.1:n.2658G>A
ENST00000694889.1:n.1733G>A
ENST00000694890.1:n.1378G>A
ENST00000694908.1:c.*1135G>A	ENSP00000511584.1:n.*1135G>A
ENST00000694909.1:c.*1135G>A	ENSP00000511585.1:n.*1135G>A
ENST00000694910.1:n.5089G>A
ENST00000694911.1:c.*3597G>A	ENSP00000511586.1:n.*3597G>A
ENST00000694913.1:c.*1135G>A	ENSP00000511588.1:n.*1135G>A
ENST00000694915.1:c.*1149G>A	ENSP00000511590.1:n.*1149G>A
ENST00000694916.1:c.*1222G>A	ENSP00000511591.1:n.*1222G>A
ENST00000520817.6:c.*1135G>A	ENSP00000429480.2:n.*1135G>A
ENST00000521417.6:n.1385G>A
ENST00000523128.2:n.1923G>A
ENST00000687203.1:c.*1135G>A	ENSP00000510742.1:n.*1135G>A
ENST00000357743.9:c.*1135G>A MANE Select	ENSP00000350378.4:n.*1135G>A
ENST00000357743.8:c.*1135G>A	ENSP00000350378.4:n.*1135G>A
ENST00000405786.2:c.*1149G>A	ENSP00000386030.2:n.*1149G>A
ENST00000520817.5:c.*1135G>A	ENSP00000429480.1:n.*1135G>A
NM_001002296.1:c.*1135G>A	NP_001002296.1:n.*1135G>A
NM_001174124.1:c.*1149G>A	NP_001167595.1:n.*1149G>A
NM_016099.2:c.*1135G>A	NP_057183.2:n.*1135G>A
NM_001362979.1:c.*1135G>A	NP_001349908.1:n.*1135G>A
NM_001362980.1:c.*1135G>A	NP_001349909.1:n.*1135G>A
NR_156425.1:n.1612G>A
NR_156426.1:n.1590G>A
NR_156427.1:n.1494G>A
NM_001002296.2:c.*1135G>A MANE Select	NP_001002296.1:n.*1135G>A
NM_001174124.2:c.*1149G>A	NP_001167595.1:n.*1149G>A
NM_001362980.2:c.*1135G>A	NP_001349909.1:n.*1135G>A
NM_016099.3:c.*1135G>A	NP_057183.2:n.*1135G>A
NR_156425.2:n.1642G>A
NR_156426.2:n.1570G>A
NR_156427.2:n.1474G>A