Canonical Allele Identifier: CA515473332

Gene: PHKA2

Linked Data

• MyVariant Identifiers: chrX:g.18969334G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18951216G>T , CM000685.2:g.18951216G>T	GRCh38
NC_000023.10:g.18969334G>T , CM000685.1:g.18969334G>T	GRCh37
NC_000023.9:g.18879255G>T	NCBI36
NG_016622.1:g.38147C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.342C>A MANE Select	ENSP00000369274.4:p.Ala114=
ENST00000379942.4:c.342C>A	ENSP00000369274.4:p.Ala114=
NM_000292.2:c.342C>A	NP_000283.1:p.Ala114=
XM_005274548.3:c.342C>A	XP_005274605.1:p.Ala114=
XM_005274550.3:c.342C>A	XP_005274607.1:p.Ala114=
XM_006724496.2:c.342C>A	XP_006724559.1:p.Ala114=
XM_006724498.2:c.-93+1278C>A	XP_006724561.1:n.-93+1278C>A
XM_011545537.1:c.342C>A	XP_011543839.1:p.Ala114=
XR_950461.1:n.526C>A
XM_005274548.5:c.342C>A	XP_005274605.1:p.Ala114=
XM_005274550.5:c.342C>A	XP_005274607.1:p.Ala114=
XM_006724496.4:c.342C>A	XP_006724559.1:p.Ala114=
XM_006724498.4:c.-93+1278C>A	XP_006724561.1:n.-93+1278C>A
XM_011545537.3:c.342C>A	XP_011543839.1:p.Ala114=
XR_001755697.2:n.512C>A
XR_001755698.2:n.512C>A
XR_002958777.1:n.512C>A
XR_950461.3:n.512C>A
NM_000292.3:c.342C>A MANE Select	NP_000283.1:p.Ala114=