Canonical Allele Identifier: CA412375390

Gene: PHKA2

Linked Data

• MyVariant Identifiers: chrX:g.18969312C>A (hg19) ; chrX:g.18951194C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18951194C>A , CM000685.2:g.18951194C>A	GRCh38
NC_000023.10:g.18969312C>A , CM000685.1:g.18969312C>A	GRCh37
NC_000023.9:g.18879233C>A	NCBI36
NG_016622.1:g.38169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.364G>T MANE Select	ENSP00000369274.4:p.Gly122Cys
ENST00000379942.4:c.364G>T	ENSP00000369274.4:p.Gly122Cys
NM_000292.2:c.364G>T	NP_000283.1:p.Gly122Cys
XM_005274548.3:c.364G>T	XP_005274605.1:p.Gly122Cys
XM_005274550.3:c.364G>T	XP_005274607.1:p.Gly122Cys
XM_006724496.2:c.364G>T	XP_006724559.1:p.Gly122Cys
XM_006724498.2:c.-93+1300G>T	XP_006724561.1:n.-93+1300G>T
XM_011545537.1:c.364G>T	XP_011543839.1:p.Gly122Cys
XR_950461.1:n.548G>T
XM_005274548.5:c.364G>T	XP_005274605.1:p.Gly122Cys
XM_005274550.5:c.364G>T	XP_005274607.1:p.Gly122Cys
XM_006724496.4:c.364G>T	XP_006724559.1:p.Gly122Cys
XM_006724498.4:c.-93+1300G>T	XP_006724561.1:n.-93+1300G>T
XM_011545537.3:c.364G>T	XP_011543839.1:p.Gly122Cys
XR_001755697.2:n.534G>T
XR_001755698.2:n.534G>T
XR_002958777.1:n.534G>T
XR_950461.3:n.534G>T
NM_000292.3:c.364G>T MANE Select	NP_000283.1:p.Gly122Cys