Canonical Allele Identifier: CA412374659

Gene: PHKA2 PHKA2-AS1

Linked Data

• dbSNP Id: rs1336244483
• gnomAD v3: X-18893640-T-C
• gnomAD v4: X-18893640-T-C
• MyVariant Identifiers: chrX:g.18911758T>C (hg19) ; chrX:g.18893640T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893640T>C , CM000685.2:g.18893640T>C	GRCh38
NC_000023.10:g.18911758T>C , CM000685.1:g.18911758T>C	GRCh37
NC_000023.9:g.18821679T>C	NCBI36
NG_016622.1:g.95723A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3553A>G (PHKA2) MANE Select	ENSP00000369274.4:p.Met1185Val
ENST00000379942.4:c.3553A>G (PHKA2)	ENSP00000369274.4:p.Met1185Val
ENST00000469485.5:n.1278A>G (PHKA2)
ENST00000473597.1:n.322A>G (PHKA2)
ENST00000481718.1:n.2447A>G (PHKA2)
NM_000292.2:c.3553A>G (PHKA2)	NP_000283.1:p.Met1185Val
NR_029379.1:n.467+302T>C (PHKA2-AS1)
XM_005274548.3:c.3499A>G (PHKA2)	XP_005274605.1:p.Met1167Val
XM_005274550.3:c.3469A>G (PHKA2)	XP_005274607.1:p.Met1157Val
XM_006724496.2:c.3577A>G (PHKA2)	XP_006724559.1:p.Met1193Val
XM_006724498.2:c.3031A>G (PHKA2)	XP_006724561.1:p.Met1011Val
XM_011545537.1:c.3478A>G (PHKA2)	XP_011543839.1:p.Met1160Val
XM_011545538.1:c.2560A>G (PHKA2)	XP_011543840.1:p.Met854Val
XM_005274548.5:c.3499A>G (PHKA2)	XP_005274605.1:p.Met1167Val
XM_005274550.5:c.3469A>G (PHKA2)	XP_005274607.1:p.Met1157Val
XM_006724496.4:c.3577A>G (PHKA2)	XP_006724559.1:p.Met1193Val
XM_006724498.4:c.3031A>G (PHKA2)	XP_006724561.1:p.Met1011Val
XM_011545537.3:c.3478A>G (PHKA2)	XP_011543839.1:p.Met1160Val
XM_011545538.3:c.2560A>G (PHKA2)	XP_011543840.1:p.Met854Val
XM_017029580.2:c.2671A>G (PHKA2)	XP_016885069.1:p.Met891Val
XR_001755698.2:n.5681A>G (PHKA2)
NM_000292.3:c.3553A>G (PHKA2) MANE Select	NP_000283.1:p.Met1185Val