Canonical Allele Identifier: CA349704526

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178326733A>T (hg19) ; chr2:g.177462005A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177462005A>T , CM000664.2:g.177462005A>T	GRCh38
NC_000002.11:g.178326733A>T , CM000664.1:g.178326733A>T	GRCh37
NC_000002.10:g.178034979A>T	NCBI36
NG_008968.1:g.74263A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.983A>T MANE Select	ENSP00000264167.4:p.Asn328Ile
ENST00000460342.2:n.2395A>T
ENST00000637633.2:c.983A>T	ENSP00000490844.2:p.Asn328Ile
ENST00000642466.2:c.983A>T	ENSP00000494433.2:p.Asn328Ile
ENST00000679421.1:n.2212A>T
ENST00000679459.1:c.983A>T	ENSP00000506137.1:p.Asn328Ile
ENST00000679478.1:c.713A>T	ENSP00000506484.1:p.Asn238Ile
ENST00000679639.1:n.786A>T
ENST00000679994.1:c.713A>T	ENSP00000504957.1:p.Asn238Ile
ENST00000680028.1:n.2347A>T
ENST00000680155.1:c.713A>T	ENSP00000505333.1:p.Asn238Ile
ENST00000680705.1:n.1027A>T
ENST00000680770.1:c.983A>T	ENSP00000505536.1:p.Asn328Ile
ENST00000680893.1:c.*231A>T	ENSP00000505929.1:n.*231A>T
ENST00000680910.1:n.1013A>T
ENST00000681028.1:c.713A>T	ENSP00000506323.1:p.Asn238Ile
ENST00000681032.1:c.*361A>T	ENSP00000505205.1:n.*361A>T
ENST00000681449.1:c.713A>T	ENSP00000505342.1:p.Asn238Ile
ENST00000681565.1:c.983A>T	ENSP00000505620.1:p.Asn328Ile
ENST00000681752.1:c.*753A>T	ENSP00000504994.1:n.*753A>T
ENST00000681891.1:n.4727A>T
ENST00000264167.8:c.983A>T	ENSP00000264167.4:p.Asn328Ile
ENST00000409888.1:c.350+41647A>T	ENSP00000386688.1:n.350+41647A>T
NM_003659.3:c.983A>T	NP_003650.1:p.Asn328Ile
XM_011512041.1:c.713A>T	XP_011510343.1:p.Asn238Ile
XM_011512042.1:c.713A>T	XP_011510344.1:p.Asn238Ile
XM_011512043.1:c.248A>T	XP_011510345.1:p.Asn83Ile
XM_011512044.1:c.983A>T	XP_011510346.1:p.Asn328Ile
XM_011512045.1:c.983A>T	XP_011510347.1:p.Asn328Ile
XM_011512041.2:c.713A>T	XP_011510343.1:p.Asn238Ile
XM_011512043.2:c.248A>T	XP_011510345.1:p.Asn83Ile
XR_001739007.2:n.1000A>T
NM_003659.4:c.983A>T MANE Select	NP_003650.1:p.Asn328Ile