Canonical Allele Identifier: CA2436816631
Community Standard Title: NM_002637.4(PHKA1):c.*1991A=
Gene: PHKA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72579011T= , CM000685.2:g.72579011T= GRCh38
NC_000023.10:g.71798861T= , CM000685.1:g.71798861T= GRCh37
NC_000023.9:g.71715586T= NCBI36
NG_016599.1:g.140169A=
NG_016599.2:g.140171A=

Transcript Alleles

HGVS Amino-acid Change
NM_002637.4:c.*1991A= MANE Select NP_002628.2:n.*1991A=
ENST00000373542.9:c.*1991A= MANE Select ENSP00000362643.4:n.*1991A=
NM_001122670.1:c.*1991A= NP_001116142.1:n.*1991A=
NM_001122670.2:c.*1991A= NP_001116142.1:n.*1991A=
NM_001172436.1:c.*1991A= NP_001165907.1:n.*1991A=
NM_001172436.2:c.*1991A= NP_001165907.1:n.*1991A=
NM_002637.3:c.*1991A= NP_002628.2:n.*1991A=
ENST00000339490.7:c.*1991A= ENSP00000342469.3:n.*1991A=
ENST00000373542.8:c.*1991A= ENSP00000362643.4:n.*1991A=
ENST00000373545.7:c.*1991A= ENSP00000362646.3:n.*1991A=
ENST00000541944.5:c.*1991A= ENSP00000441251.1:n.*1991A=
XM_006724661.2:c.*1991A= XP_006724724.1:n.*1991A=
XR_001755696.1:n.6593A=