Canonical Allele Identifier: CA2418091457
Gene: PHKA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18951164G= , CM000685.2:g.18951164G= GRCh38
NC_000023.10:g.18969282G= , CM000685.1:g.18969282G= GRCh37
NC_000023.9:g.18879203G= NCBI36
NG_016622.1:g.38199C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379942.5:c.394C= MANE Select ENSP00000369274.4:p.His132=
ENST00000379942.4:c.394C= ENSP00000369274.4:p.His132=
NM_000292.2:c.394C= NP_000283.1:p.His132=
XM_005274548.3:c.394C= XP_005274605.1:p.His132=
XM_005274550.3:c.394C= XP_005274607.1:p.His132=
XM_006724496.2:c.394C= XP_006724559.1:p.His132=
XM_006724498.2:c.-93+1330C= XP_006724561.1:n.-93+1330C=
XM_011545537.1:c.394C= XP_011543839.1:p.His132=
XR_950461.1:n.578C=
XM_005274548.5:c.394C= XP_005274605.1:p.His132=
XM_005274550.5:c.394C= XP_005274607.1:p.His132=
XM_006724496.4:c.394C= XP_006724559.1:p.His132=
XM_006724498.4:c.-93+1330C= XP_006724561.1:n.-93+1330C=
XM_011545537.3:c.394C= XP_011543839.1:p.His132=
XM_017029580.2:c.-448C= XP_016885069.1:n.-448C=
XR_001755697.2:n.564C=
XR_001755698.2:n.564C=
XR_002958777.1:n.564C=
XR_950461.3:n.564C=
NM_000292.3:c.394C= MANE Select NP_000283.1:p.His132=