Canonical Allele Identifier: CA369549483

Gene: AGK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141611229A>T , CM000669.2:g.141611229A>T	GRCh38
NC_000007.13:g.141311029A>T , CM000669.1:g.141311029A>T	GRCh37
NC_000007.12:g.140957498A>T	NCBI36
NG_032079.1:g.64952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647568.1:c.332A>T	ENSP00000497039.1:p.Glu111Val
ENST00000647898.1:n.222A>T
ENST00000648068.1:c.332A>T	ENSP00000498112.1:p.Glu111Val
ENST00000648395.1:c.56A>T	ENSP00000497666.1:p.Glu19Val
ENST00000648489.1:n.363A>T
ENST00000648690.1:c.56A>T	ENSP00000497945.1:p.Glu19Val
ENST00000649014.1:c.332A>T	ENSP00000497984.1:p.Glu111Val
ENST00000649286.2:c.332A>T MANE Select	ENSP00000497280.1:p.Glu111Val
ENST00000649365.1:c.*340A>T	ENSP00000496835.1:n.*340A>T
ENST00000649538.1:n.360A>T
ENST00000649790.1:c.56A>T	ENSP00000498193.1:p.Glu19Val
ENST00000649914.1:c.320A>T	ENSP00000497848.1:p.Glu107Val
ENST00000650006.1:c.332A>T	ENSP00000497457.1:p.Glu111Val
ENST00000650365.1:c.*217A>T	ENSP00000497358.1:n.*217A>T
ENST00000650547.1:c.332A>T	ENSP00000496789.1:p.Glu111Val
ENST00000355413.8:c.332A>T	ENSP00000347581.4:p.Glu111Val
ENST00000465241.5:n.343A>T
ENST00000473247.5:c.248A>T	ENSP00000420776.1:p.Glu83Val
ENST00000473884.5:c.*151A>T	ENSP00000420540.1:n.*151A>T
ENST00000494688.1:c.323A>T	ENSP00000418101.1:p.Glu108Val
ENST00000496273.1:n.95A>T
ENST00000629555.2:c.323A>T	ENSP00000487274.1:p.Glu108Val
NM_018238.3:c.332A>T	NP_060708.1:p.Glu111Val
XM_005250023.3:c.332A>T	XP_005250080.1:p.Glu111Val
XM_011516397.1:c.332A>T	XP_011514699.1:p.Glu111Val
NM_001364948.1:c.332A>T	NP_001351877.1:p.Glu111Val
NM_018238.4:c.332A>T MANE Select	NP_060708.1:p.Glu111Val
XM_011516397.3:c.332A>T	XP_011514699.1:p.Glu111Val
XM_024446835.1:c.332A>T	XP_024302603.1:p.Glu111Val
NM_001364948.2:c.332A>T	NP_001351877.1:p.Glu111Val
NM_001364948.3:c.332A>T	NP_001351877.1:p.Glu111Val