Canonical Allele Identifier: CA2662079545

Gene: AGPS

Linked Data

• gnomAD v4: 2-177462025-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177462030del , CM000664.2:g.177462030del	GRCh38
NC_000002.11:g.178326758del , CM000664.1:g.178326758del	GRCh37
NC_000002.10:g.178035004del	NCBI36
NG_008968.1:g.74288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.996+12del MANE Select	ENSP00000264167.4:n.996+12del
ENST00000460342.2:n.2420del
ENST00000637633.2:c.996+12del	ENSP00000490844.2:n.996+12del
ENST00000642466.2:c.996+12del	ENSP00000494433.2:n.996+12del
ENST00000679421.1:n.2225+12del
ENST00000679459.1:c.996+12del	ENSP00000506137.1:n.996+12del
ENST00000679478.1:c.726+12del	ENSP00000506484.1:n.726+12del
ENST00000679639.1:n.811del
ENST00000679994.1:c.726+12del	ENSP00000504957.1:n.726+12del
ENST00000680028.1:n.2360+12del
ENST00000680155.1:c.726+12del	ENSP00000505333.1:n.726+12del
ENST00000680705.1:n.1040+12del
ENST00000680770.1:c.996+12del	ENSP00000505536.1:n.996+12del
ENST00000680893.1:c.*244+12del	ENSP00000505929.1:n.*244+12del
ENST00000680910.1:n.1026+12del
ENST00000681028.1:c.726+12del	ENSP00000506323.1:n.726+12del
ENST00000681032.1:c.*374+12del	ENSP00000505205.1:n.*374+12del
ENST00000681449.1:c.726+12del	ENSP00000505342.1:n.726+12del
ENST00000681565.1:c.996+12del	ENSP00000505620.1:n.996+12del
ENST00000681752.1:c.*766+12del	ENSP00000504994.1:n.*766+12del
ENST00000681891.1:n.4740+12del
ENST00000264167.8:c.996+12del	ENSP00000264167.4:n.996+12del
ENST00000409888.1:c.350+41672del	ENSP00000386688.1:n.350+41672del
NM_003659.3:c.996+12del	NP_003650.1:n.996+12del
XM_011512041.1:c.726+12del	XP_011510343.1:n.726+12del
XM_011512042.1:c.726+12del	XP_011510344.1:n.726+12del
XM_011512043.1:c.261+12del	XP_011510345.1:n.261+12del
XM_011512044.1:c.996+12del	XP_011510346.1:n.996+12del
XM_011512045.1:c.996+12del	XP_011510347.1:n.996+12del
XM_011512041.2:c.726+12del	XP_011510343.1:n.726+12del
XM_011512043.2:c.261+12del	XP_011510345.1:n.261+12del
XR_001739007.2:n.1013+12del
NM_003659.4:c.996+12del MANE Select	NP_003650.1:n.996+12del