Canonical Allele Identifier: CA349373800

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178386008C>G (hg19) ; chr2:g.177521280C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521280C>G , CM000664.2:g.177521280C>G	GRCh38
NC_000002.11:g.178386008C>G , CM000664.1:g.178386008C>G	GRCh37
NC_000002.10:g.178094254C>G	NCBI36
NG_008968.1:g.133538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1709C>G MANE Select	ENSP00000264167.4:p.Thr570Ser
ENST00000637633.2:c.1709C>G	ENSP00000490844.2:p.Thr570Ser
ENST00000642466.2:c.1709C>G	ENSP00000494433.2:p.Thr570Ser
ENST00000679421.1:n.2938C>G
ENST00000679459.1:c.1709C>G	ENSP00000506137.1:p.Thr570Ser
ENST00000679478.1:c.1439C>G	ENSP00000506484.1:p.Thr480Ser
ENST00000679994.1:c.1439C>G	ENSP00000504957.1:p.Thr480Ser
ENST00000680028.1:n.3073C>G
ENST00000680155.1:c.1439C>G	ENSP00000505333.1:p.Thr480Ser
ENST00000680390.1:n.744C>G
ENST00000680770.1:c.1709C>G	ENSP00000505536.1:p.Thr570Ser
ENST00000680893.1:c.*957C>G	ENSP00000505929.1:n.*957C>G
ENST00000681028.1:c.*136C>G	ENSP00000506323.1:n.*136C>G
ENST00000681032.1:c.*1087C>G	ENSP00000505205.1:n.*1087C>G
ENST00000681300.1:n.664C>G
ENST00000681449.1:c.1439C>G	ENSP00000505342.1:p.Thr480Ser
ENST00000681565.1:c.*842C>G	ENSP00000505620.1:n.*842C>G
ENST00000681752.1:c.*1479C>G	ENSP00000504994.1:n.*1479C>G
ENST00000681891.1:n.5344C>G
ENST00000264167.8:c.1709C>G	ENSP00000264167.4:p.Thr570Ser
ENST00000409888.1:c.351-49C>G	ENSP00000386688.1:n.351-49C>G
NM_003659.3:c.1709C>G	NP_003650.1:p.Thr570Ser
XM_011512041.1:c.1439C>G	XP_011510343.1:p.Thr480Ser
XM_011512042.1:c.1439C>G	XP_011510344.1:p.Thr480Ser
XM_011512043.1:c.974C>G	XP_011510345.1:p.Thr325Ser
XM_011512041.2:c.1439C>G	XP_011510343.1:p.Thr480Ser
XM_011512043.2:c.974C>G	XP_011510345.1:p.Thr325Ser
XR_001739007.2:n.1617C>G
NM_003659.4:c.1709C>G MANE Select	NP_003650.1:p.Thr570Ser