Canonical Allele Identifier: CA3038188359

Gene: PHKA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72579052T>A , CM000685.2:g.72579052T>A	GRCh38
NC_000023.10:g.71798902T>A , CM000685.1:g.71798902T>A	GRCh37
NC_000023.9:g.71715627T>A	NCBI36
NG_016599.1:g.140128A>T
NG_016599.2:g.140130A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002637.4:c.*1950A>T MANE Select	NP_002628.2:n.*1950A>T
ENST00000373542.9:c.*1950A>T MANE Select	ENSP00000362643.4:n.*1950A>T
NM_001122670.1:c.*1950A>T	NP_001116142.1:n.*1950A>T
NM_001122670.2:c.*1950A>T	NP_001116142.1:n.*1950A>T
NM_001172436.1:c.*1950A>T	NP_001165907.1:n.*1950A>T
NM_001172436.2:c.*1950A>T	NP_001165907.1:n.*1950A>T
NM_002637.3:c.*1950A>T	NP_002628.2:n.*1950A>T
ENST00000339490.7:c.*1950A>T	ENSP00000342469.3:n.*1950A>T
ENST00000373542.8:c.*1950A>T	ENSP00000362643.4:n.*1950A>T
ENST00000373545.7:c.*1950A>T	ENSP00000362646.3:n.*1950A>T
ENST00000541944.5:c.*1950A>T	ENSP00000441251.1:n.*1950A>T
XM_006724661.2:c.*1950A>T	XP_006724724.1:n.*1950A>T
XR_001755696.1:n.6552A>T