Canonical Allele Identifier: CA1748088802

Gene: AGK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141611228G= , CM000669.2:g.141611228G=	GRCh38
NC_000007.13:g.141311028G= , CM000669.1:g.141311028G=	GRCh37
NC_000007.12:g.140957497G=	NCBI36
NG_032079.1:g.64951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.331G=	ENSP00000497039.1:p.Glu111=
ENST00000647898.1:n.221G=
ENST00000648068.1:c.331G=	ENSP00000498112.1:p.Glu111=
ENST00000648395.1:c.55G=	ENSP00000497666.1:p.Glu19=
ENST00000648489.1:n.362G=
ENST00000648690.1:c.55G=	ENSP00000497945.1:p.Glu19=
ENST00000649014.1:c.331G=	ENSP00000497984.1:p.Glu111=
ENST00000649286.2:c.331G= MANE Select	ENSP00000497280.1:p.Glu111=
ENST00000649365.1:c.*339G=	ENSP00000496835.1:n.*339G=
ENST00000649538.1:n.359G=
ENST00000649790.1:c.55G=	ENSP00000498193.1:p.Glu19=
ENST00000649914.1:c.319G=	ENSP00000497848.1:p.Glu107=
ENST00000650006.1:c.331G=	ENSP00000497457.1:p.Glu111=
ENST00000650365.1:c.*216G=	ENSP00000497358.1:n.*216G=
ENST00000650547.1:c.331G=	ENSP00000496789.1:p.Glu111=
ENST00000355413.8:c.331G=	ENSP00000347581.4:p.Glu111=
ENST00000465241.5:n.342G=
ENST00000473247.5:c.247G=	ENSP00000420776.1:p.Glu83=
ENST00000473884.5:c.*150G=	ENSP00000420540.1:n.*150G=
ENST00000494688.1:c.322G=	ENSP00000418101.1:p.Glu108=
ENST00000496273.1:n.94G=
ENST00000629555.2:c.322G=	ENSP00000487274.1:p.Glu108=
NM_018238.3:c.331G=	NP_060708.1:p.Glu111=
XM_005250023.3:c.331G=	XP_005250080.1:p.Glu111=
XM_011516397.1:c.331G=	XP_011514699.1:p.Glu111=
NM_001364948.1:c.331G=	NP_001351877.1:p.Glu111=
NM_018238.4:c.331G= MANE Select	NP_060708.1:p.Glu111=
XM_011516397.3:c.331G=	XP_011514699.1:p.Glu111=
XM_024446835.1:c.331G=	XP_024302603.1:p.Glu111=
NM_001364948.2:c.331G=	NP_001351877.1:p.Glu111=
NM_001364948.3:c.331G=	NP_001351877.1:p.Glu111=