Canonical Allele Identifier: CA578270510
Gene: AGK HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141596548C>G , CM000669.2:g.141596548C>G GRCh38
NC_000007.13:g.141296348C>G , CM000669.1:g.141296348C>G GRCh37
NC_000007.12:g.140942817C>G NCBI36
NG_032079.1:g.50271C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647568.1:c.142-14C>G ENSP00000497039.1:n.142-14C>G
ENST00000647898.1:n.32-14C>G
ENST00000648068.1:c.142-14C>G ENSP00000498112.1:n.142-14C>G
ENST00000648395.1:c.-135-14C>G ENSP00000497666.1:n.-135-14C>G
ENST00000648489.1:n.173-14C>G
ENST00000648690.1:c.-135-14C>G ENSP00000497945.1:n.-135-14C>G
ENST00000649014.1:c.142-14C>G ENSP00000497984.1:n.142-14C>G
ENST00000649286.2:c.142-14C>G MANE Select ENSP00000497280.1:n.142-14C>G
ENST00000649365.1:c.*150-14C>G ENSP00000496835.1:n.*150-14C>G
ENST00000649538.1:n.170-14C>G
ENST00000649790.1:c.-135-14C>G ENSP00000498193.1:n.-135-14C>G
ENST00000649914.1:c.130-14C>G ENSP00000497848.1:n.130-14C>G
ENST00000650006.1:c.142-14C>G ENSP00000497457.1:n.142-14C>G
ENST00000650365.1:c.102-14C>G ENSP00000497358.1:n.102-14C>G
ENST00000650547.1:c.142-14C>G ENSP00000496789.1:n.142-14C>G
ENST00000355413.8:c.142-14C>G ENSP00000347581.4:n.142-14C>G
ENST00000465241.5:n.153-14C>G
ENST00000473247.5:c.58-14C>G ENSP00000420776.1:n.58-14C>G
ENST00000473884.5:c.102-14C>G ENSP00000420540.1:n.102-14C>G
ENST00000494688.1:c.142-14C>G ENSP00000418101.1:n.142-14C>G
ENST00000495028.5:n.181-14C>G
ENST00000496784.1:n.143-14C>G
ENST00000629555.2:c.142-14C>G ENSP00000487274.1:n.142-14C>G
NM_018238.3:c.142-14C>G NP_060708.1:n.142-14C>G
XM_005250023.3:c.142-14C>G XP_005250080.1:n.142-14C>G
XM_011516397.1:c.142-14C>G XP_011514699.1:n.142-14C>G
NM_001364948.1:c.142-14C>G NP_001351877.1:n.142-14C>G
NM_018238.4:c.142-14C>G MANE Select NP_060708.1:n.142-14C>G
XM_011516397.3:c.142-14C>G XP_011514699.1:n.142-14C>G
XM_024446835.1:c.142-14C>G XP_024302603.1:n.142-14C>G
NM_001364948.2:c.142-14C>G NP_001351877.1:n.142-14C>G
NM_001364948.3:c.142-14C>G NP_001351877.1:n.142-14C>G