Canonical Allele Identifier: CA2436843932
Gene: PHKA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72667251T= , CM000685.2:g.72667251T= GRCh38
NC_000023.10:g.71887101T= , CM000685.1:g.71887101T= GRCh37
NC_000023.9:g.71803826T= NCBI36
NG_016599.1:g.51929A=
NG_016599.2:g.51931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373542.9:c.717+124A= MANE Select ENSP00000362643.4:n.717+124A=
ENST00000339490.7:c.717+124A= ENSP00000342469.3:n.717+124A=
ENST00000373539.3:c.717+124A= ENSP00000362640.3:n.717+124A=
ENST00000373542.8:c.717+124A= ENSP00000362643.4:n.717+124A=
ENST00000373545.7:c.717+124A= ENSP00000362646.3:n.717+124A=
ENST00000541944.5:c.717+124A= ENSP00000441251.1:n.717+124A=
NM_001122670.1:c.717+124A= NP_001116142.1:n.717+124A=
NM_001172436.1:c.717+124A= NP_001165907.1:n.717+124A=
NM_002637.3:c.717+124A= NP_002628.2:n.717+124A=
XM_006724661.2:c.717+124A= XP_006724724.1:n.717+124A=
XR_001755696.1:n.860+124A=
NM_002637.4:c.717+124A= MANE Select NP_002628.2:n.717+124A=
NM_001122670.2:c.717+124A= NP_001116142.1:n.717+124A=
NM_001172436.2:c.717+124A= NP_001165907.1:n.717+124A=