Canonical Allele Identifier: CA1778994738
Gene: GOLGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41510699C= , CM000670.2:g.41510699C= GRCh38
NC_000008.10:g.41368218C= , CM000670.1:g.41368218C= GRCh37
NC_000008.9:g.41487375C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405786.3:c.*1145C= ENSP00000386030.2:n.*1145C=
ENST00000518270.6:c.*1131C= ENSP00000429329.1:n.*1131C=
ENST00000694863.1:c.*1131C= ENSP00000511547.1:n.*1131C=
ENST00000694872.1:c.*1131C= ENSP00000511557.1:n.*1131C=
ENST00000694873.1:c.*1131C= ENSP00000511558.1:n.*1131C=
ENST00000694874.1:c.*1131C= ENSP00000511559.1:n.*1131C=
ENST00000694875.1:c.*1131C= ENSP00000511560.1:n.*1131C=
ENST00000694876.1:c.*981C= ENSP00000511561.1:n.*981C=
ENST00000694877.1:c.*1145C= ENSP00000511562.1:n.*1145C=
ENST00000694878.1:c.*1145C= ENSP00000511563.1:n.*1145C=
ENST00000694879.1:n.1402C=
ENST00000694883.1:c.*1145C= ENSP00000511567.1:n.*1145C=
ENST00000694884.1:c.*1205C= ENSP00000511568.1:n.*1205C=
ENST00000694885.1:n.2652C=
ENST00000694886.1:c.*1131C= ENSP00000511569.1:n.*1131C=
ENST00000694887.1:c.*1131C= ENSP00000511570.1:n.*1131C=
ENST00000694888.1:n.2654C=
ENST00000694889.1:n.1729C=
ENST00000694890.1:n.1374C=
ENST00000694908.1:c.*1131C= ENSP00000511584.1:n.*1131C=
ENST00000694909.1:c.*1131C= ENSP00000511585.1:n.*1131C=
ENST00000694910.1:n.5085C=
ENST00000694911.1:c.*3593C= ENSP00000511586.1:n.*3593C=
ENST00000694913.1:c.*1131C= ENSP00000511588.1:n.*1131C=
ENST00000694915.1:c.*1145C= ENSP00000511590.1:n.*1145C=
ENST00000694916.1:c.*1218C= ENSP00000511591.1:n.*1218C=
ENST00000520817.6:c.*1131C= ENSP00000429480.2:n.*1131C=
ENST00000521417.6:n.1381C=
ENST00000523128.2:n.1919C=
ENST00000687203.1:c.*1131C= ENSP00000510742.1:n.*1131C=
ENST00000357743.9:c.*1131C= MANE Select ENSP00000350378.4:n.*1131C=
ENST00000357743.8:c.*1131C= ENSP00000350378.4:n.*1131C=
ENST00000405786.2:c.*1145C= ENSP00000386030.2:n.*1145C=
ENST00000520817.5:c.*1131C= ENSP00000429480.1:n.*1131C=
NM_001002296.1:c.*1131C= NP_001002296.1:n.*1131C=
NM_001174124.1:c.*1145C= NP_001167595.1:n.*1145C=
NM_016099.2:c.*1131C= NP_057183.2:n.*1131C=
NM_001362979.1:c.*1131C= NP_001349908.1:n.*1131C=
NM_001362980.1:c.*1131C= NP_001349909.1:n.*1131C=
NR_156425.1:n.1608C=
NR_156426.1:n.1586C=
NR_156427.1:n.1490C=
NM_001002296.2:c.*1131C= MANE Select NP_001002296.1:n.*1131C=
NM_001174124.2:c.*1145C= NP_001167595.1:n.*1145C=
NM_001362980.2:c.*1131C= NP_001349909.1:n.*1131C=
NM_016099.3:c.*1131C= NP_057183.2:n.*1131C=
NR_156425.2:n.1638C=
NR_156426.2:n.1566C=
NR_156427.2:n.1470C=