Canonical Allele Identifier: CA412375178
Gene: PHKA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18951168C>G , CM000685.2:g.18951168C>G GRCh38
NC_000023.10:g.18969286C>G , CM000685.1:g.18969286C>G GRCh37
NC_000023.9:g.18879207C>G NCBI36
NG_016622.1:g.38195G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379942.5:c.390G>C MANE Select ENSP00000369274.4:p.Trp130Cys
ENST00000379942.4:c.390G>C ENSP00000369274.4:p.Trp130Cys
NM_000292.2:c.390G>C NP_000283.1:p.Trp130Cys
XM_005274548.3:c.390G>C XP_005274605.1:p.Trp130Cys
XM_005274550.3:c.390G>C XP_005274607.1:p.Trp130Cys
XM_006724496.2:c.390G>C XP_006724559.1:p.Trp130Cys
XM_006724498.2:c.-93+1326G>C XP_006724561.1:n.-93+1326G>C
XM_011545537.1:c.390G>C XP_011543839.1:p.Trp130Cys
XR_950461.1:n.574G>C
XM_005274548.5:c.390G>C XP_005274605.1:p.Trp130Cys
XM_005274550.5:c.390G>C XP_005274607.1:p.Trp130Cys
XM_006724496.4:c.390G>C XP_006724559.1:p.Trp130Cys
XM_006724498.4:c.-93+1326G>C XP_006724561.1:n.-93+1326G>C
XM_011545537.3:c.390G>C XP_011543839.1:p.Trp130Cys
XM_017029580.2:c.-452G>C XP_016885069.1:n.-452G>C
XR_001755697.2:n.560G>C
XR_001755698.2:n.560G>C
XR_002958777.1:n.560G>C
XR_950461.3:n.560G>C
NM_000292.3:c.390G>C MANE Select NP_000283.1:p.Trp130Cys