Canonical Allele Identifier: CA516753833

Gene: PHKA1

Linked Data

• MyVariant Identifiers: chrX:g.71887285A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72667435A>G , CM000685.2:g.72667435A>G	GRCh38
NC_000023.10:g.71887285A>G , CM000685.1:g.71887285A>G	GRCh37
NC_000023.9:g.71804010A>G	NCBI36
NG_016599.1:g.51745T>C
NG_016599.2:g.51747T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373542.9:c.657T>C MANE Select	ENSP00000362643.4:p.Gly219=
ENST00000339490.7:c.657T>C	ENSP00000342469.3:p.Gly219=
ENST00000373539.3:c.657T>C	ENSP00000362640.3:p.Gly219=
ENST00000373542.8:c.657T>C	ENSP00000362643.4:p.Gly219=
ENST00000373545.7:c.657T>C	ENSP00000362646.3:p.Gly219=
ENST00000541944.5:c.657T>C	ENSP00000441251.1:p.Gly219=
NM_001122670.1:c.657T>C	NP_001116142.1:p.Gly219=
NM_001172436.1:c.657T>C	NP_001165907.1:p.Gly219=
NM_002637.3:c.657T>C	NP_002628.2:p.Gly219=
XM_006724661.2:c.657T>C	XP_006724724.1:p.Gly219=
XR_001755696.1:n.800T>C
NM_002637.4:c.657T>C MANE Select	NP_002628.2:p.Gly219=
NM_001122670.2:c.657T>C	NP_001116142.1:p.Gly219=
NM_001172436.2:c.657T>C	NP_001165907.1:p.Gly219=