Canonical Allele Identifier: CA622395962
Gene: PHKB HGNC NCBI

Linked Data

dbSNP Id: rs5816579

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47698618_47698622dup , CM000678.2:g.47698618_47698622dup GRCh38
NC_000016.9:g.47732529_47732533dup , CM000678.1:g.47732529_47732533dup GRCh37
NC_000016.8:g.46290030_46290034dup NCBI36
NG_016598.1:g.242320_242324dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696809.1:c.*1718+30_*1718+34dup ENSP00000512887.1:n.*1718+30_*1718+34dup
ENST00000699276.1:c.*772+30_*772+34dup ENSP00000514257.1:n.*772+30_*772+34dup
ENST00000323584.10:c.3144+30_3144+34dup MANE Select ENSP00000313504.5:n.3144+30_3144+34dup
ENST00000299167.12:c.3144+30_3144+34dup ENSP00000299167.8:n.3144+30_3144+34dup
ENST00000323584.9:c.3144+30_3144+34dup ENSP00000313504.5:n.3144+30_3144+34dup
ENST00000564711.2:c.158+30_158+34dup
ENST00000566044.5:c.3123+30_3123+34dup ENSP00000456729.1:n.3123+30_3123+34dup
ENST00000566319.2:n.1960+30_1960+34dup
NM_000293.2:c.3144+30_3144+34dup NP_000284.1:n.3144+30_3144+34dup
NM_001031835.2:c.3123+30_3123+34dup NP_001027005.1:n.3123+30_3123+34dup
XM_005255983.3:c.3144+30_3144+34dup XP_005256040.1:n.3144+30_3144+34dup
XM_005255984.3:c.3123+30_3123+34dup XP_005256041.1:n.3123+30_3123+34dup
XM_011523107.1:c.1722+30_1722+34dup XP_011521409.1:n.1722+30_1722+34dup
NM_001363837.1:c.3144+30_3144+34dup NP_001350766.1:n.3144+30_3144+34dup
XM_005255983.4:c.3144+30_3144+34dup XP_005256040.1:n.3144+30_3144+34dup
XM_005255984.4:c.3123+30_3123+34dup XP_005256041.1:n.3123+30_3123+34dup
XM_017023282.1:c.2031+30_2031+34dup XP_016878771.1:n.2031+30_2031+34dup
XM_017023283.1:c.1722+30_1722+34dup XP_016878772.1:n.1722+30_1722+34dup
XM_017023284.1:c.1722+30_1722+34dup XP_016878773.1:n.1722+30_1722+34dup
XR_001751913.1:n.3068+30_3068+34dup
NM_000293.3:c.3144+30_3144+34dup MANE Select NP_000284.1:n.3144+30_3144+34dup
NM_001031835.3:c.3123+30_3123+34dup NP_001027005.1:n.3123+30_3123+34dup