Canonical Allele Identifier: CA1980001

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177392853G>A , CM000664.2:g.177392853G>A	GRCh38
NC_000002.11:g.178257581G>A , CM000664.1:g.178257581G>A	GRCh37
NC_000002.10:g.177965827G>A	NCBI36
NG_008968.1:g.5111G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003659.4:c.64G>A MANE Select	NP_003650.1:p.Ala22Thr
ENST00000264167.11:c.64G>A MANE Select	ENSP00000264167.4:p.Ala22Thr
NM_003659.3:c.64G>A	NP_003650.1:p.Ala22Thr
ENST00000264167.8:c.64G>A	ENSP00000264167.4:p.Ala22Thr
ENST00000409888.1:c.64G>A	ENSP00000386688.1:p.Ala22Thr
ENST00000460342.2:n.106G>A
ENST00000637633.2:c.64G>A	ENSP00000490844.2:p.Ala22Thr
ENST00000642466.2:c.64G>A	ENSP00000494433.2:p.Ala22Thr
ENST00000679421.1:n.94G>A
ENST00000679459.1:c.64G>A	ENSP00000506137.1:p.Ala22Thr
ENST00000680677.1:n.94G>A
ENST00000680705.1:n.108G>A
ENST00000680770.1:c.64G>A	ENSP00000505536.1:p.Ala22Thr
ENST00000680893.1:c.64G>A	ENSP00000505929.1:p.Ala22Thr
ENST00000680910.1:n.94G>A
ENST00000681032.1:c.64G>A	ENSP00000505205.1:p.Ala22Thr
ENST00000681565.1:c.64G>A	ENSP00000505620.1:p.Ala22Thr
ENST00000681752.1:c.64G>A	ENSP00000504994.1:p.Ala22Thr
XM_011512044.1:c.64G>A	XP_011510346.1:p.Ala22Thr
XM_011512045.1:c.64G>A	XP_011510347.1:p.Ala22Thr
XR_001739007.2:n.81G>A