Canonical Allele Identifier: CA10361679
Community Standard Title: NM_000292.3(PHKA2):c.2257G>A (p.Asp753Asn)
Gene: PHKA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18908904C>T , CM000685.2:g.18908904C>T GRCh38
NC_000023.10:g.18927022C>T , CM000685.1:g.18927022C>T GRCh37
NC_000023.9:g.18836943C>T NCBI36
NG_016622.1:g.80459G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000292.3:c.2257G>A MANE Select NP_000283.1:p.Asp753Asn
ENST00000379942.5:c.2257G>A MANE Select ENSP00000369274.4:p.Asp753Asn
NM_000292.2:c.2257G>A NP_000283.1:p.Asp753Asn
ENST00000379942.4:c.2257G>A ENSP00000369274.4:p.Asp753Asn
XM_005274548.3:c.2257G>A XP_005274605.1:p.Asp753Asn
XM_005274548.5:c.2257G>A XP_005274605.1:p.Asp753Asn
XM_005274550.3:c.2257G>A XP_005274607.1:p.Asp753Asn
XM_005274550.5:c.2257G>A XP_005274607.1:p.Asp753Asn
XM_006724496.2:c.2257G>A XP_006724559.1:p.Asp753Asn
XM_006724496.4:c.2257G>A XP_006724559.1:p.Asp753Asn
XM_006724498.2:c.1711G>A XP_006724561.1:p.Asp571Asn
XM_006724498.4:c.1711G>A XP_006724561.1:p.Asp571Asn
XM_011545537.1:c.2158G>A XP_011543839.1:p.Asp720Asn
XM_011545537.3:c.2158G>A XP_011543839.1:p.Asp720Asn
XM_011545538.1:c.1240G>A XP_011543840.1:p.Asp414Asn
XM_011545538.3:c.1240G>A XP_011543840.1:p.Asp414Asn
XM_017029580.2:c.1351G>A XP_016885069.1:p.Asp451Asn
XR_001755697.2:n.2427G>A
XR_001755698.2:n.2427G>A
XR_002958777.1:n.2427G>A
XR_950461.1:n.2441G>A
XR_950461.3:n.2427G>A