Canonical Allele Identifier: CA495361406

Gene: PHKB

Linked Data

• COSMIC: COSM3509784 ; COSM3509786
• MyVariant Identifiers: chr16:g.47730372G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696461G>A , CM000678.2:g.47696461G>A	GRCh38
NC_000016.9:g.47730372G>A , CM000678.1:g.47730372G>A	GRCh37
NC_000016.8:g.46287873G>A	NCBI36
NG_016598.1:g.240163G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1550G>A	ENSP00000512887.1:n.*1550G>A
ENST00000699276.1:c.*604G>A	ENSP00000514257.1:n.*604G>A
ENST00000323584.10:c.2976G>A MANE Select	ENSP00000313504.5:p.Gln992=
ENST00000299167.12:c.2976G>A	ENSP00000299167.8:p.Gln992=
ENST00000323584.9:c.2976G>A	ENSP00000313504.5:p.Gln992=
ENST00000566044.5:c.2955G>A	ENSP00000456729.1:p.Gln985=
ENST00000566319.2:n.1792G>A
NM_000293.2:c.2976G>A	NP_000284.1:p.Gln992=
NM_001031835.2:c.2955G>A	NP_001027005.1:p.Gln985=
XM_005255983.3:c.2976G>A	XP_005256040.1:p.Gln992=
XM_005255984.3:c.2955G>A	XP_005256041.1:p.Gln985=
XM_011523107.1:c.1554G>A	XP_011521409.1:p.Gln518=
NM_001363837.1:c.2976G>A	NP_001350766.1:p.Gln992=
XM_005255983.4:c.2976G>A	XP_005256040.1:p.Gln992=
XM_005255984.4:c.2955G>A	XP_005256041.1:p.Gln985=
XM_017023282.1:c.1863G>A	XP_016878771.1:p.Gln621=
XM_017023283.1:c.1554G>A	XP_016878772.1:p.Gln518=
XM_017023284.1:c.1554G>A	XP_016878773.1:p.Gln518=
XR_001751913.1:n.2900G>A
NM_000293.3:c.2976G>A MANE Select	NP_000284.1:p.Gln992=
NM_001031835.3:c.2955G>A	NP_001027005.1:p.Gln985=