Canonical Allele Identifier: CA642480993

Gene: PHKA1

Linked Data

• dbSNP Id: rs1556306837
• gnomAD v2: X-71887183-C-A
• gnomAD v4: X-72667333-C-A
• MyVariant Identifiers: chrX:g.71887183C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72667333C>A , CM000685.2:g.72667333C>A	GRCh38
NC_000023.10:g.71887183C>A , CM000685.1:g.71887183C>A	GRCh37
NC_000023.9:g.71803908C>A	NCBI36
NG_016599.1:g.51847G>T
NG_016599.2:g.51849G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373542.9:c.717+42G>T MANE Select	ENSP00000362643.4:n.717+42G>T
ENST00000339490.7:c.717+42G>T	ENSP00000342469.3:n.717+42G>T
ENST00000373539.3:c.717+42G>T	ENSP00000362640.3:n.717+42G>T
ENST00000373542.8:c.717+42G>T	ENSP00000362643.4:n.717+42G>T
ENST00000373545.7:c.717+42G>T	ENSP00000362646.3:n.717+42G>T
ENST00000541944.5:c.717+42G>T	ENSP00000441251.1:n.717+42G>T
NM_001122670.1:c.717+42G>T	NP_001116142.1:n.717+42G>T
NM_001172436.1:c.717+42G>T	NP_001165907.1:n.717+42G>T
NM_002637.3:c.717+42G>T	NP_002628.2:n.717+42G>T
XM_006724661.2:c.717+42G>T	XP_006724724.1:n.717+42G>T
XR_001755696.1:n.860+42G>T
NM_002637.4:c.717+42G>T MANE Select	NP_002628.2:n.717+42G>T
NM_001122670.2:c.717+42G>T	NP_001116142.1:n.717+42G>T
NM_001172436.2:c.717+42G>T	NP_001165907.1:n.717+42G>T