Canonical Allele Identifier: CA622395992
Gene: PHKB HGNC NCBI

Linked Data

dbSNP Id: rs1277443531

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47698634_47698635del , CM000678.2:g.47698634_47698635del GRCh38
NC_000016.9:g.47732545_47732546del , CM000678.1:g.47732545_47732546del GRCh37
NC_000016.8:g.46290046_46290047del NCBI36
NG_016598.1:g.242336_242337del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696809.1:c.*1718+46_*1718+47del ENSP00000512887.1:n.*1718+46_*1718+47del
ENST00000699276.1:c.*772+46_*772+47del ENSP00000514257.1:n.*772+46_*772+47del
ENST00000323584.10:c.3144+46_3144+47del MANE Select ENSP00000313504.5:n.3144+46_3144+47del
ENST00000299167.12:c.3144+46_3144+47del ENSP00000299167.8:n.3144+46_3144+47del
ENST00000323584.9:c.3144+46_3144+47del ENSP00000313504.5:n.3144+46_3144+47del
ENST00000564711.2:c.158+46_158+47del
ENST00000566044.5:c.3123+46_3123+47del ENSP00000456729.1:n.3123+46_3123+47del
ENST00000566319.2:n.1960+46_1960+47del
NM_000293.2:c.3144+46_3144+47del NP_000284.1:n.3144+46_3144+47del
NM_001031835.2:c.3123+46_3123+47del NP_001027005.1:n.3123+46_3123+47del
XM_005255983.3:c.3144+46_3144+47del XP_005256040.1:n.3144+46_3144+47del
XM_005255984.3:c.3123+46_3123+47del XP_005256041.1:n.3123+46_3123+47del
XM_011523107.1:c.1722+46_1722+47del XP_011521409.1:n.1722+46_1722+47del
NM_001363837.1:c.3144+46_3144+47del NP_001350766.1:n.3144+46_3144+47del
XM_005255983.4:c.3144+46_3144+47del XP_005256040.1:n.3144+46_3144+47del
XM_005255984.4:c.3123+46_3123+47del XP_005256041.1:n.3123+46_3123+47del
XM_017023282.1:c.2031+46_2031+47del XP_016878771.1:n.2031+46_2031+47del
XM_017023283.1:c.1722+46_1722+47del XP_016878772.1:n.1722+46_1722+47del
XM_017023284.1:c.1722+46_1722+47del XP_016878773.1:n.1722+46_1722+47del
XR_001751913.1:n.3068+46_3068+47del
NM_000293.3:c.3144+46_3144+47del MANE Select NP_000284.1:n.3144+46_3144+47del
NM_001031835.3:c.3123+46_3123+47del NP_001027005.1:n.3123+46_3123+47del