Canonical Allele Identifier: CA2685260809
Gene: AGK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141641184G>A , CM000669.2:g.141641184G>A GRCh38
NC_000007.13:g.141340984G>A , CM000669.1:g.141340984G>A GRCh37
NC_000007.12:g.140987453G>A NCBI36
NG_032079.1:g.94907G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647568.1:c.*690-64G>A ENSP00000497039.1:n.*690-64G>A
ENST00000648068.1:c.727-64G>A ENSP00000498112.1:n.727-64G>A
ENST00000648395.1:c.451-64G>A ENSP00000497666.1:n.451-64G>A
ENST00000648489.1:n.758-64G>A
ENST00000649014.1:c.*2-64G>A ENSP00000497984.1:n.*2-64G>A
ENST00000649286.2:c.727-64G>A MANE Select ENSP00000497280.1:n.727-64G>A
ENST00000649365.1:c.*735-64G>A ENSP00000496835.1:n.*735-64G>A
ENST00000649790.1:c.*163-64G>A ENSP00000498193.1:n.*163-64G>A
ENST00000649914.1:c.715-64G>A ENSP00000497848.1:n.715-64G>A
ENST00000650006.1:c.727-64G>A ENSP00000497457.1:n.727-64G>A
ENST00000650365.1:c.*612-64G>A ENSP00000497358.1:n.*612-64G>A
ENST00000650547.1:c.727-64G>A ENSP00000496789.1:n.727-64G>A
ENST00000355413.8:c.727-64G>A ENSP00000347581.4:n.727-64G>A
ENST00000473247.5:c.643-64G>A ENSP00000420776.1:n.643-64G>A
ENST00000494688.1:c.718-627G>A ENSP00000418101.1:n.718-627G>A
ENST00000629555.2:c.718-627G>A ENSP00000487274.1:n.718-627G>A
NM_018238.3:c.727-64G>A NP_060708.1:n.727-64G>A
XM_005250023.3:c.727-64G>A XP_005250080.1:n.727-64G>A
XM_011516397.1:c.727-64G>A XP_011514699.1:n.727-64G>A
NM_001364948.1:c.727-64G>A NP_001351877.1:n.727-64G>A
NM_018238.4:c.727-64G>A MANE Select NP_060708.1:n.727-64G>A
XM_011516397.3:c.727-64G>A XP_011514699.1:n.727-64G>A
XM_024446835.1:c.727-64G>A XP_024302603.1:n.727-64G>A
NM_001364948.2:c.727-64G>A NP_001351877.1:n.727-64G>A
NM_001364948.3:c.727-64G>A NP_001351877.1:n.727-64G>A