Canonical Allele Identifier: CA413594538

Gene: PHKA1

Linked Data

• MyVariant Identifiers: chrX:g.71887287C>G (hg19) ; chrX:g.72667437C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72667437C>G , CM000685.2:g.72667437C>G	GRCh38
NC_000023.10:g.71887287C>G , CM000685.1:g.71887287C>G	GRCh37
NC_000023.9:g.71804012C>G	NCBI36
NG_016599.1:g.51743G>C
NG_016599.2:g.51745G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373542.9:c.655G>C MANE Select	ENSP00000362643.4:p.Gly219Arg
ENST00000339490.7:c.655G>C	ENSP00000342469.3:p.Gly219Arg
ENST00000373539.3:c.655G>C	ENSP00000362640.3:p.Gly219Arg
ENST00000373542.8:c.655G>C	ENSP00000362643.4:p.Gly219Arg
ENST00000373545.7:c.655G>C	ENSP00000362646.3:p.Gly219Arg
ENST00000541944.5:c.655G>C	ENSP00000441251.1:p.Gly219Arg
NM_001122670.1:c.655G>C	NP_001116142.1:p.Gly219Arg
NM_001172436.1:c.655G>C	NP_001165907.1:p.Gly219Arg
NM_002637.3:c.655G>C	NP_002628.2:p.Gly219Arg
XM_006724661.2:c.655G>C	XP_006724724.1:p.Gly219Arg
XR_001755696.1:n.798G>C
NM_002637.4:c.655G>C MANE Select	NP_002628.2:p.Gly219Arg
NM_001122670.2:c.655G>C	NP_001116142.1:p.Gly219Arg
NM_001172436.2:c.655G>C	NP_001165907.1:p.Gly219Arg