Canonical Allele Identifier: CA1882341783
Gene: AK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132742950G= , CM000671.2:g.132742950G= GRCh38
NC_000009.11:g.135618337G= , CM000671.1:g.135618337G= GRCh37
NC_000009.10:g.134608158G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000298545.4:c.1122-15416C= MANE Select ENSP00000298545.3:n.1122-15416C=
ENST00000298545.3:c.1122-15416C= ENSP00000298545.3:n.1122-15416C=
ENST00000476719.1:n.1559-15416C=
ENST00000477396.5:n.2037-15416C=
NM_152572.2:c.1122-15416C= NP_689785.1:n.1122-15416C=
XM_005272169.2:c.1158-15416C= XP_005272226.1:n.1158-15416C=
XM_006716964.2:c.987-15416C= XP_006717027.1:n.987-15416C=
XM_006716965.2:c.906-15416C= XP_006717028.1:n.906-15416C=
XM_011518278.1:c.900-15416C= XP_011516580.1:n.900-15416C=
XM_011518279.1:c.606-15416C= XP_011516581.1:n.606-15416C=
XM_011518280.1:c.510-15416C= XP_011516582.1:n.510-15416C=
XR_929719.1:n.1075-15416C=
NM_001317958.1:c.510-15416C= NP_001304887.1:n.510-15416C=
NM_001317959.1:c.606-15416C= NP_001304888.1:n.606-15416C=
XM_011518278.2:c.900-15416C= XP_011516580.1:n.900-15416C=
XM_017014308.1:c.606-15416C= XP_016869797.1:n.606-15416C=
XM_024447419.1:c.510-15416C= XP_024303187.1:n.510-15416C=
XM_024447420.1:c.510-15416C= XP_024303188.1:n.510-15416C=
XR_929719.2:n.1075-15416C=
NM_001317958.2:c.510-15416C= NP_001304887.1:n.510-15416C=
NM_001317959.2:c.606-15416C= NP_001304888.1:n.606-15416C=
NM_001371771.1:c.1035-15416C= NP_001358700.1:n.1035-15416C=
NM_001371772.1:c.987-15416C= NP_001358701.1:n.987-15416C=
NM_001371773.1:c.510-15416C= NP_001358702.1:n.510-15416C=
NM_001371774.1:c.510-15416C= NP_001358703.1:n.510-15416C=
NM_152572.3:c.1122-15416C= MANE Select NP_689785.1:n.1122-15416C=