Canonical Allele Identifier: CA396101147

Gene: PHKB

Linked Data

• MyVariant Identifiers: chr16:g.47730365T>A (hg19) ; chr16:g.47696454T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696454T>A , CM000678.2:g.47696454T>A	GRCh38
NC_000016.9:g.47730365T>A , CM000678.1:g.47730365T>A	GRCh37
NC_000016.8:g.46287866T>A	NCBI36
NG_016598.1:g.240156T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1543T>A	ENSP00000512887.1:n.*1543T>A
ENST00000699276.1:c.*597T>A	ENSP00000514257.1:n.*597T>A
ENST00000323584.10:c.2969T>A MANE Select	ENSP00000313504.5:p.Ile990Asn
ENST00000299167.12:c.2969T>A	ENSP00000299167.8:p.Ile990Asn
ENST00000323584.9:c.2969T>A	ENSP00000313504.5:p.Ile990Asn
ENST00000566044.5:c.2948T>A	ENSP00000456729.1:p.Ile983Asn
ENST00000566319.2:n.1785T>A
NM_000293.2:c.2969T>A	NP_000284.1:p.Ile990Asn
NM_001031835.2:c.2948T>A	NP_001027005.1:p.Ile983Asn
XM_005255983.3:c.2969T>A	XP_005256040.1:p.Ile990Asn
XM_005255984.3:c.2948T>A	XP_005256041.1:p.Ile983Asn
XM_011523107.1:c.1547T>A	XP_011521409.1:p.Ile516Asn
NM_001363837.1:c.2969T>A	NP_001350766.1:p.Ile990Asn
XM_005255983.4:c.2969T>A	XP_005256040.1:p.Ile990Asn
XM_005255984.4:c.2948T>A	XP_005256041.1:p.Ile983Asn
XM_017023282.1:c.1856T>A	XP_016878771.1:p.Ile619Asn
XM_017023283.1:c.1547T>A	XP_016878772.1:p.Ile516Asn
XM_017023284.1:c.1547T>A	XP_016878773.1:p.Ile516Asn
XR_001751913.1:n.2893T>A
NM_000293.3:c.2969T>A MANE Select	NP_000284.1:p.Ile990Asn
NM_001031835.3:c.2948T>A	NP_001027005.1:p.Ile983Asn