Canonical Allele Identifier: CA2436816969
Gene: PHKA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72579704G= , CM000685.2:g.72579704G= GRCh38
NC_000023.10:g.71799554G= , CM000685.1:g.71799554G= GRCh37
NC_000023.9:g.71716279G= NCBI36
NG_016599.1:g.139476C=
NG_016599.2:g.139478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373542.9:c.*1298C= MANE Select ENSP00000362643.4:n.*1298C=
ENST00000339490.7:c.*1298C= ENSP00000342469.3:n.*1298C=
ENST00000373542.8:c.*1298C= ENSP00000362643.4:n.*1298C=
ENST00000373545.7:c.*1298C= ENSP00000362646.3:n.*1298C=
ENST00000541944.5:c.*1298C= ENSP00000441251.1:n.*1298C=
NM_001122670.1:c.*1298C= NP_001116142.1:n.*1298C=
NM_001172436.1:c.*1298C= NP_001165907.1:n.*1298C=
NM_002637.3:c.*1298C= NP_002628.2:n.*1298C=
XM_006724661.2:c.*1298C= XP_006724724.1:n.*1298C=
XR_001755696.1:n.5900C=
NM_002637.4:c.*1298C= MANE Select NP_002628.2:n.*1298C=
NM_001122670.2:c.*1298C= NP_001116142.1:n.*1298C=
NM_001172436.2:c.*1298C= NP_001165907.1:n.*1298C=