Canonical Allele Identifier: CA349704419

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178326687T>A (hg19) ; chr2:g.177461959T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177461959T>A , CM000664.2:g.177461959T>A	GRCh38
NC_000002.11:g.178326687T>A , CM000664.1:g.178326687T>A	GRCh37
NC_000002.10:g.178034933T>A	NCBI36
NG_008968.1:g.74217T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264167.11:c.937T>A MANE Select	ENSP00000264167.4:p.Trp313Arg
ENST00000460342.2:n.2349T>A
ENST00000637633.2:c.937T>A	ENSP00000490844.2:p.Trp313Arg
ENST00000642466.2:c.937T>A	ENSP00000494433.2:p.Trp313Arg
ENST00000679421.1:n.2166T>A
ENST00000679459.1:c.937T>A	ENSP00000506137.1:p.Trp313Arg
ENST00000679478.1:c.667T>A	ENSP00000506484.1:p.Trp223Arg
ENST00000679639.1:n.740T>A
ENST00000679994.1:c.667T>A	ENSP00000504957.1:p.Trp223Arg
ENST00000680028.1:n.2301T>A
ENST00000680155.1:c.667T>A	ENSP00000505333.1:p.Trp223Arg
ENST00000680705.1:n.981T>A
ENST00000680770.1:c.937T>A	ENSP00000505536.1:p.Trp313Arg
ENST00000680893.1:c.*185T>A	ENSP00000505929.1:n.*185T>A
ENST00000680910.1:n.967T>A
ENST00000681028.1:c.667T>A	ENSP00000506323.1:p.Trp223Arg
ENST00000681032.1:c.*315T>A	ENSP00000505205.1:n.*315T>A
ENST00000681449.1:c.667T>A	ENSP00000505342.1:p.Trp223Arg
ENST00000681565.1:c.937T>A	ENSP00000505620.1:p.Trp313Arg
ENST00000681752.1:c.*707T>A	ENSP00000504994.1:n.*707T>A
ENST00000681891.1:n.4681T>A
ENST00000264167.8:c.937T>A	ENSP00000264167.4:p.Trp313Arg
ENST00000409888.1:c.350+41601T>A	ENSP00000386688.1:n.350+41601T>A
NM_003659.3:c.937T>A	NP_003650.1:p.Trp313Arg
XM_011512041.1:c.667T>A	XP_011510343.1:p.Trp223Arg
XM_011512042.1:c.667T>A	XP_011510344.1:p.Trp223Arg
XM_011512043.1:c.202T>A	XP_011510345.1:p.Trp68Arg
XM_011512044.1:c.937T>A	XP_011510346.1:p.Trp313Arg
XM_011512045.1:c.937T>A	XP_011510347.1:p.Trp313Arg
XM_011512041.2:c.667T>A	XP_011510343.1:p.Trp223Arg
XM_011512043.2:c.202T>A	XP_011510345.1:p.Trp68Arg
XR_001739007.2:n.954T>A
NM_003659.4:c.937T>A MANE Select	NP_003650.1:p.Trp313Arg