Canonical Allele Identifier: CA2753310261

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177461767_177461768insTTTTTTTGA , CM000664.2:g.177461767_177461768insTTTTTTTGA	GRCh38
NC_000002.11:g.178326495_178326496insTTTTTTTGA , CM000664.1:g.178326495_178326496insTTTTTTTGA	GRCh37
NC_000002.10:g.178034741_178034742insTTTTTTTGA	NCBI36
NG_008968.1:g.74025_74026insTTTTTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.871-126_871-125insTTTTTTTGA MANE Select	ENSP00000264167.4:n.871-126_871-125insTTTTTTTGA
ENST00000460342.2:n.2283-126_2283-125insTTTTTTTGA
ENST00000637633.2:c.871-126_871-125insTTTTTTTGA	ENSP00000490844.2:n.871-126_871-125insTTTTTTTGA
ENST00000642466.2:c.871-126_871-125insTTTTTTTGA	ENSP00000494433.2:n.871-126_871-125insTTTTTTTGA
ENST00000679421.1:n.2100-126_2100-125insTTTTTTTGA
ENST00000679459.1:c.871-126_871-125insTTTTTTTGA	ENSP00000506137.1:n.871-126_871-125insTTTTTTTGA
ENST00000679478.1:c.601-126_601-125insTTTTTTTGA	ENSP00000506484.1:n.601-126_601-125insTTTTTTTGA
ENST00000679639.1:n.674-126_674-125insTTTTTTTGA
ENST00000679994.1:c.601-126_601-125insTTTTTTTGA	ENSP00000504957.1:n.601-126_601-125insTTTTTTTGA
ENST00000680028.1:n.2235-126_2235-125insTTTTTTTGA
ENST00000680155.1:c.601-126_601-125insTTTTTTTGA	ENSP00000505333.1:n.601-126_601-125insTTTTTTTGA
ENST00000680705.1:n.915-126_915-125insTTTTTTTGA
ENST00000680770.1:c.871-126_871-125insTTTTTTTGA	ENSP00000505536.1:n.871-126_871-125insTTTTTTTGA
ENST00000680893.1:c.*119-126_*119-125insTTTTTTTGA	ENSP00000505929.1:n.*119-126_*119-125insTTTTTTTGA
ENST00000680910.1:n.901-126_901-125insTTTTTTTGA
ENST00000681028.1:c.601-126_601-125insTTTTTTTGA	ENSP00000506323.1:n.601-126_601-125insTTTTTTTGA
ENST00000681032.1:c.*249-126_*249-125insTTTTTTTGA	ENSP00000505205.1:n.*249-126_*249-125insTTTTTTTGA
ENST00000681449.1:c.601-126_601-125insTTTTTTTGA	ENSP00000505342.1:n.601-126_601-125insTTTTTTTGA
ENST00000681565.1:c.871-126_871-125insTTTTTTTGA	ENSP00000505620.1:n.871-126_871-125insTTTTTTTGA
ENST00000681752.1:c.*641-126_*641-125insTTTTTTTGA	ENSP00000504994.1:n.*641-126_*641-125insTTTTTTTGA
ENST00000681891.1:n.4615-126_4615-125insTTTTTTTGA
ENST00000264167.8:c.871-126_871-125insTTTTTTTGA	ENSP00000264167.4:n.871-126_871-125insTTTTTTTGA
ENST00000409888.1:c.350+41409_350+41410insTTTTTTTGA	ENSP00000386688.1:n.350+41409_350+41410insTTTTTTTGA
NM_003659.3:c.871-126_871-125insTTTTTTTGA	NP_003650.1:n.871-126_871-125insTTTTTTTGA
XM_011512041.1:c.601-126_601-125insTTTTTTTGA	XP_011510343.1:n.601-126_601-125insTTTTTTTGA
XM_011512042.1:c.601-126_601-125insTTTTTTTGA	XP_011510344.1:n.601-126_601-125insTTTTTTTGA
XM_011512043.1:c.136-126_136-125insTTTTTTTGA	XP_011510345.1:n.136-126_136-125insTTTTTTTGA
XM_011512044.1:c.871-126_871-125insTTTTTTTGA	XP_011510346.1:n.871-126_871-125insTTTTTTTGA
XM_011512045.1:c.871-126_871-125insTTTTTTTGA	XP_011510347.1:n.871-126_871-125insTTTTTTTGA
XM_011512041.2:c.601-126_601-125insTTTTTTTGA	XP_011510343.1:n.601-126_601-125insTTTTTTTGA
XM_011512043.2:c.136-126_136-125insTTTTTTTGA	XP_011510345.1:n.136-126_136-125insTTTTTTTGA
XR_001739007.2:n.888-126_888-125insTTTTTTTGA
NM_003659.4:c.871-126_871-125insTTTTTTTGA MANE Select	NP_003650.1:n.871-126_871-125insTTTTTTTGA