Canonical Allele Identifier: CA2309652

Gene: GOLGA4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37326718T>G , CM000665.2:g.37326718T>G	GRCh38
NC_000003.11:g.37368209T>G , CM000665.1:g.37368209T>G	GRCh37
NC_000003.10:g.37343213T>G	NCBI36
NG_047053.1:g.88528T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431105.2:c.4997T>G	ENSP00000392907.2:p.Val1666Gly
ENST00000437131.2:c.4898T>G	ENSP00000405842.2:p.Val1633Gly
ENST00000699994.1:c.4898T>G	ENSP00000514744.1:p.Val1633Gly
ENST00000699995.1:c.4898T>G	ENSP00000514745.1:p.Val1633Gly
ENST00000699996.1:c.4898T>G	ENSP00000514746.1:p.Val1633Gly
ENST00000706569.1:c.4997T>G	ENSP00000516454.1:p.Val1666Gly
ENST00000361924.7:c.4832T>G MANE Select	ENSP00000354486.2:p.Val1611Gly
ENST00000356847.8:c.4898T>G	ENSP00000349305.4:p.Val1633Gly
ENST00000361924.6:c.4832T>G	ENSP00000354486.2:p.Val1611Gly
ENST00000437131.1:c.4445T>G	ENSP00000405842.1:p.Val1482Gly
ENST00000444882.5:c.478-39362T>G	ENSP00000406894.1:n.478-39362T>G
NM_001172713.1:c.4898T>G	NP_001166184.1:p.Val1633Gly
NM_002078.4:c.4832T>G	NP_002069.2:p.Val1611Gly
XM_005265069.3:c.4997T>G	XP_005265126.1:p.Val1666Gly
XM_005265070.3:c.4997T>G	XP_005265127.1:p.Val1666Gly
XM_005265071.3:c.4997T>G	XP_005265128.1:p.Val1666Gly
XM_005265072.3:c.4949T>G	XP_005265129.1:p.Val1650Gly
XM_005265073.1:c.4898T>G	XP_005265130.1:p.Val1633Gly
XM_005265074.1:c.4898T>G	XP_005265131.1:p.Val1633Gly
XM_005265075.1:c.4784T>G	XP_005265132.1:p.Val1595Gly
XM_006713110.2:c.4892T>G	XP_006713173.1:p.Val1631Gly
XM_011533597.1:c.4475T>G	XP_011531899.1:p.Val1492Gly
XM_011533598.1:c.3521T>G	XP_011531900.1:p.Val1174Gly
XM_011533598.3:c.3521T>G	XP_011531900.1:p.Val1174Gly
XM_017006184.1:c.4997T>G	XP_016861673.1:p.Val1666Gly
XM_017006185.1:c.4895T>G	XP_016861674.1:p.Val1632Gly
XM_017006186.1:c.4895T>G	XP_016861675.1:p.Val1632Gly
XM_017006187.1:c.4850T>G	XP_016861676.1:p.Val1617Gly
XM_017006188.1:c.4727T>G	XP_016861677.1:p.Val1576Gly
XM_024453456.1:c.4475T>G	XP_024309224.1:p.Val1492Gly
XM_024453457.1:c.4475T>G	XP_024309225.1:p.Val1492Gly
XM_024453458.1:c.4427T>G	XP_024309226.1:p.Val1476Gly
NM_001172713.2:c.4898T>G	NP_001166184.1:p.Val1633Gly
NM_002078.5:c.4832T>G MANE Select	NP_002069.2:p.Val1611Gly