Canonical Allele Identifier: CA537782938

Gene: AGPS

Linked Data

• dbSNP Id: rs1300742724
• gnomAD v2: 2-178385612-TAACAA-T
• gnomAD v3: 2-177520884-TAACAA-T
• gnomAD v4: 2-177520884-TAACAA-T
• MyVariant Identifiers: chr2:g.178385613_178385617del (hg19) ; chr2:g.177520885_177520889del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177520890_177520894del , CM000664.2:g.177520890_177520894del	GRCh38
NC_000002.11:g.178385618_178385622del , CM000664.1:g.178385618_178385622del	GRCh37
NC_000002.10:g.178093864_178093868del	NCBI36
NG_008968.1:g.133148_133152del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1698-379_1698-375del MANE Select	ENSP00000264167.4:n.1698-379_1698-375del
ENST00000637633.2:c.1698-379_1698-375del	ENSP00000490844.2:n.1698-379_1698-375del
ENST00000642466.2:c.1698-379_1698-375del	ENSP00000494433.2:n.1698-379_1698-375del
ENST00000679421.1:n.2927-379_2927-375del
ENST00000679459.1:c.1698-379_1698-375del	ENSP00000506137.1:n.1698-379_1698-375del
ENST00000679478.1:c.1428-379_1428-375del	ENSP00000506484.1:n.1428-379_1428-375del
ENST00000679994.1:c.1428-379_1428-375del	ENSP00000504957.1:n.1428-379_1428-375del
ENST00000680028.1:n.3062-379_3062-375del
ENST00000680155.1:c.1428-379_1428-375del	ENSP00000505333.1:n.1428-379_1428-375del
ENST00000680390.1:n.733-379_733-375del
ENST00000680770.1:c.1698-379_1698-375del	ENSP00000505536.1:n.1698-379_1698-375del
ENST00000680893.1:c.*946-379_*946-375del	ENSP00000505929.1:n.*946-379_*946-375del
ENST00000681028.1:c.*125-379_*125-375del	ENSP00000506323.1:n.*125-379_*125-375del
ENST00000681032.1:c.*1076-379_*1076-375del	ENSP00000505205.1:n.*1076-379_*1076-375del
ENST00000681300.1:n.653-379_653-375del
ENST00000681449.1:c.1428-379_1428-375del	ENSP00000505342.1:n.1428-379_1428-375del
ENST00000681565.1:c.*831-379_*831-375del	ENSP00000505620.1:n.*831-379_*831-375del
ENST00000681752.1:c.*1468-379_*1468-375del	ENSP00000504994.1:n.*1468-379_*1468-375del
ENST00000681891.1:n.5333-379_5333-375del
ENST00000264167.8:c.1698-379_1698-375del	ENSP00000264167.4:n.1698-379_1698-375del
ENST00000409888.1:c.351-439_351-435del	ENSP00000386688.1:n.351-439_351-435del
NM_003659.3:c.1698-379_1698-375del	NP_003650.1:n.1698-379_1698-375del
XM_011512041.1:c.1428-379_1428-375del	XP_011510343.1:n.1428-379_1428-375del
XM_011512042.1:c.1428-379_1428-375del	XP_011510344.1:n.1428-379_1428-375del
XM_011512043.1:c.963-379_963-375del	XP_011510345.1:n.963-379_963-375del
XM_011512041.2:c.1428-379_1428-375del	XP_011510343.1:n.1428-379_1428-375del
XM_011512043.2:c.963-379_963-375del	XP_011510345.1:n.963-379_963-375del
XR_001739007.2:n.1606-379_1606-375del
NM_003659.4:c.1698-379_1698-375del MANE Select	NP_003650.1:n.1698-379_1698-375del