Canonical Allele Identifier: CA2633045838

Gene: PHKB

Linked Data

• gnomAD v4: 16-47596347-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47596347_47596348insG , CM000678.2:g.47596347_47596348insG	GRCh38
NC_000016.9:g.47630258_47630259insG , CM000678.1:g.47630258_47630259insG	GRCh37
NC_000016.8:g.46187759_46187760insG	NCBI36
NG_016598.1:g.140049_140050insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.1184-26_1184-25insG	ENSP00000512887.1:n.1184-26_1184-25insG
ENST00000699276.1:c.1184-26_1184-25insG	ENSP00000514257.1:n.1184-26_1184-25insG
ENST00000323584.10:c.1205-26_1205-25insG MANE Select	ENSP00000313504.5:n.1205-26_1205-25insG
ENST00000299167.12:c.1205-26_1205-25insG	ENSP00000299167.8:n.1205-26_1205-25insG
ENST00000323584.9:c.1205-26_1205-25insG	ENSP00000313504.5:n.1205-26_1205-25insG
ENST00000566044.5:c.1184-26_1184-25insG	ENSP00000456729.1:n.1184-26_1184-25insG
ENST00000566436.1:n.66-26_66-25insG
NM_000293.2:c.1205-26_1205-25insG	NP_000284.1:n.1205-26_1205-25insG
NM_001031835.2:c.1184-26_1184-25insG	NP_001027005.1:n.1184-26_1184-25insG
XM_005255983.3:c.1205-26_1205-25insG	XP_005256040.1:n.1205-26_1205-25insG
XM_005255984.3:c.1184-26_1184-25insG	XP_005256041.1:n.1184-26_1184-25insG
XM_011523106.1:c.1205-26_1205-25insG	XP_011521408.1:n.1205-26_1205-25insG
NM_001363837.1:c.1205-26_1205-25insG	NP_001350766.1:n.1205-26_1205-25insG
XM_005255983.4:c.1205-26_1205-25insG	XP_005256040.1:n.1205-26_1205-25insG
XM_005255984.4:c.1184-26_1184-25insG	XP_005256041.1:n.1184-26_1184-25insG
XM_017023282.1:c.92-26_92-25insG	XP_016878771.1:n.92-26_92-25insG
XM_017023283.1:c.-301-26_-301-25insG	XP_016878772.1:n.-301-26_-301-25insG
XM_017023284.1:c.-301-26_-301-25insG	XP_016878773.1:n.-301-26_-301-25insG
XR_001751913.1:n.1220-26_1220-25insG
NM_000293.3:c.1205-26_1205-25insG MANE Select	NP_000284.1:n.1205-26_1205-25insG
NM_001031835.3:c.1184-26_1184-25insG	NP_001027005.1:n.1184-26_1184-25insG