Canonical Allele Identifier: CA430060463

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178386051C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521323C>T , CM000664.2:g.177521323C>T	GRCh38
NC_000002.11:g.178386051C>T , CM000664.1:g.178386051C>T	GRCh37
NC_000002.10:g.178094297C>T	NCBI36
NG_008968.1:g.133581C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1752C>T MANE Select	ENSP00000264167.4:p.Asn584=
ENST00000637633.2:c.1752C>T	ENSP00000490844.2:p.Asn584=
ENST00000642466.2:c.1752C>T	ENSP00000494433.2:p.Asn584=
ENST00000679421.1:n.2981C>T
ENST00000679459.1:c.1752C>T	ENSP00000506137.1:p.Asn584=
ENST00000679478.1:c.1482C>T	ENSP00000506484.1:p.Asn494=
ENST00000679994.1:c.1482C>T	ENSP00000504957.1:p.Asn494=
ENST00000680028.1:n.3116C>T
ENST00000680155.1:c.1482C>T	ENSP00000505333.1:p.Asn494=
ENST00000680390.1:n.787C>T
ENST00000680770.1:c.1752C>T	ENSP00000505536.1:p.Asn584=
ENST00000680893.1:c.*1000C>T	ENSP00000505929.1:n.*1000C>T
ENST00000681028.1:c.*179C>T	ENSP00000506323.1:n.*179C>T
ENST00000681032.1:c.*1130C>T	ENSP00000505205.1:n.*1130C>T
ENST00000681300.1:n.707C>T
ENST00000681449.1:c.1482C>T	ENSP00000505342.1:p.Asn494=
ENST00000681565.1:c.*885C>T	ENSP00000505620.1:n.*885C>T
ENST00000681752.1:c.*1522C>T	ENSP00000504994.1:n.*1522C>T
ENST00000681891.1:n.5387C>T
ENST00000264167.8:c.1752C>T	ENSP00000264167.4:p.Asn584=
ENST00000409888.1:c.351-6C>T	ENSP00000386688.1:n.351-6C>T
NM_003659.3:c.1752C>T	NP_003650.1:p.Asn584=
XM_011512041.1:c.1482C>T	XP_011510343.1:p.Asn494=
XM_011512042.1:c.1482C>T	XP_011510344.1:p.Asn494=
XM_011512043.1:c.1017C>T	XP_011510345.1:p.Asn339=
XM_011512041.2:c.1482C>T	XP_011510343.1:p.Asn494=
XM_011512043.2:c.1017C>T	XP_011510345.1:p.Asn339=
XR_001739007.2:n.1660C>T
NM_003659.4:c.1752C>T MANE Select	NP_003650.1:p.Asn584=