Canonical Allele Identifier: CA2632771574

Gene: PHKG2

Linked Data

• gnomAD v4: 16-30756579-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756584_30756585del , CM000678.2:g.30756584_30756585del	GRCh38
NC_000016.9:g.30767905_30767906del , CM000678.1:g.30767905_30767906del	GRCh37
NC_000016.8:g.30675406_30675407del	NCBI36
NG_016616.1:g.13286_13287del
NG_016616.2:g.13286_13287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.802-6_802-5del MANE Select	ENSP00000455607.1:n.802-6_802-5del
ENST00000328273.11:c.814-6_814-5del	ENSP00000329968.7:n.814-6_814-5del
ENST00000424889.7:c.802-6_802-5del	ENSP00000388571.3:n.802-6_802-5del
ENST00000563588.5:c.802-6_802-5del	ENSP00000455607.1:n.802-6_802-5del
ENST00000563913.5:n.1135-6_1135-5del
ENST00000564838.5:n.931-6_931-5del
NM_000294.2:c.802-6_802-5del	NP_000285.1:n.802-6_802-5del
NM_001172432.1:c.802-6_802-5del	NP_001165903.1:n.802-6_802-5del
NM_000294.3:c.802-6_802-5del MANE Select	NP_000285.1:n.802-6_802-5del
NM_001172432.2:c.802-6_802-5del	NP_001165903.1:n.802-6_802-5del