Canonical Allele Identifier: CA2693234131

Gene: PHKA2 PHKA2-AS1

Linked Data

• gnomAD v4: X-18893671-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893671G>C , CM000685.2:g.18893671G>C	GRCh38
NC_000023.10:g.18911789G>C , CM000685.1:g.18911789G>C	GRCh37
NC_000023.9:g.18821710G>C	NCBI36
NG_016622.1:g.95692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3538-16C>G (PHKA2) MANE Select	ENSP00000369274.4:n.3538-16C>G
ENST00000379942.4:c.3538-16C>G (PHKA2)	ENSP00000369274.4:n.3538-16C>G
ENST00000469485.5:n.1263-16C>G (PHKA2)
ENST00000473597.1:n.307-16C>G (PHKA2)
ENST00000481718.1:n.2432-16C>G (PHKA2)
NM_000292.2:c.3538-16C>G (PHKA2)	NP_000283.1:n.3538-16C>G
NR_029379.1:n.467+333G>C (PHKA2-AS1)
XM_005274548.3:c.3484-16C>G (PHKA2)	XP_005274605.1:n.3484-16C>G
XM_005274550.3:c.3454-16C>G (PHKA2)	XP_005274607.1:n.3454-16C>G
XM_006724496.2:c.3562-16C>G (PHKA2)	XP_006724559.1:n.3562-16C>G
XM_006724498.2:c.3016-16C>G (PHKA2)	XP_006724561.1:n.3016-16C>G
XM_011545537.1:c.3463-16C>G (PHKA2)	XP_011543839.1:n.3463-16C>G
XM_011545538.1:c.2545-16C>G (PHKA2)	XP_011543840.1:n.2545-16C>G
XM_005274548.5:c.3484-16C>G (PHKA2)	XP_005274605.1:n.3484-16C>G
XM_005274550.5:c.3454-16C>G (PHKA2)	XP_005274607.1:n.3454-16C>G
XM_006724496.4:c.3562-16C>G (PHKA2)	XP_006724559.1:n.3562-16C>G
XM_006724498.4:c.3016-16C>G (PHKA2)	XP_006724561.1:n.3016-16C>G
XM_011545537.3:c.3463-16C>G (PHKA2)	XP_011543839.1:n.3463-16C>G
XM_011545538.3:c.2545-16C>G (PHKA2)	XP_011543840.1:n.2545-16C>G
XM_017029580.2:c.2656-16C>G (PHKA2)	XP_016885069.1:n.2656-16C>G
XR_001755698.2:n.5666-16C>G (PHKA2)
NM_000292.3:c.3538-16C>G (PHKA2) MANE Select	NP_000283.1:n.3538-16C>G