Canonical Allele Identifier: CA2694085549

Gene: PHKA1

Linked Data

• gnomAD v4: X-72579803-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72579803G>A , CM000685.2:g.72579803G>A	GRCh38
NC_000023.10:g.71799653G>A , CM000685.1:g.71799653G>A	GRCh37
NC_000023.9:g.71716378G>A	NCBI36
NG_016599.1:g.139377C>T
NG_016599.2:g.139379C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373542.9:c.*1199C>T MANE Select	ENSP00000362643.4:n.*1199C>T
ENST00000339490.7:c.*1199C>T	ENSP00000342469.3:n.*1199C>T
ENST00000373542.8:c.*1199C>T	ENSP00000362643.4:n.*1199C>T
ENST00000373545.7:c.*1199C>T	ENSP00000362646.3:n.*1199C>T
ENST00000541944.5:c.*1199C>T	ENSP00000441251.1:n.*1199C>T
NM_001122670.1:c.*1199C>T	NP_001116142.1:n.*1199C>T
NM_001172436.1:c.*1199C>T	NP_001165907.1:n.*1199C>T
NM_002637.3:c.*1199C>T	NP_002628.2:n.*1199C>T
XM_006724661.2:c.*1199C>T	XP_006724724.1:n.*1199C>T
XR_001755696.1:n.5801C>T
NM_002637.4:c.*1199C>T MANE Select	NP_002628.2:n.*1199C>T
NM_001122670.2:c.*1199C>T	NP_001116142.1:n.*1199C>T
NM_001172436.2:c.*1199C>T	NP_001165907.1:n.*1199C>T