Canonical Allele Identifier: CA2436843993

Gene: PHKA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72667484C= , CM000685.2:g.72667484C=	GRCh38
NC_000023.10:g.71887334C= , CM000685.1:g.71887334C=	GRCh37
NC_000023.9:g.71804059C=	NCBI36
NG_016599.1:g.51696G=
NG_016599.2:g.51698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373542.9:c.619-11G= MANE Select	ENSP00000362643.4:n.619-11G=
ENST00000339490.7:c.619-11G=	ENSP00000342469.3:n.619-11G=
ENST00000373539.3:c.619-11G=	ENSP00000362640.3:n.619-11G=
ENST00000373542.8:c.619-11G=	ENSP00000362643.4:n.619-11G=
ENST00000373545.7:c.619-11G=	ENSP00000362646.3:n.619-11G=
ENST00000541944.5:c.619-11G=	ENSP00000441251.1:n.619-11G=
NM_001122670.1:c.619-11G=	NP_001116142.1:n.619-11G=
NM_001172436.1:c.619-11G=	NP_001165907.1:n.619-11G=
NM_002637.3:c.619-11G=	NP_002628.2:n.619-11G=
XM_006724661.2:c.619-11G=	XP_006724724.1:n.619-11G=
XR_001755696.1:n.762-11G=
NM_002637.4:c.619-11G= MANE Select	NP_002628.2:n.619-11G=
NM_001122670.2:c.619-11G=	NP_001116142.1:n.619-11G=
NM_001172436.2:c.619-11G=	NP_001165907.1:n.619-11G=