Canonical Allele Identifier: CA2567343123

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47698622_47698623insTTAGAATTTTTTTATTTTTTTAATT , CM000678.2:g.47698622_47698623insTTAGAATTTTTTTATTTTTTTAATT	GRCh38
NC_000016.9:g.47732533_47732534insTTAGAATTTTTTTATTTTTTTAATT , CM000678.1:g.47732533_47732534insTTAGAATTTTTTTATTTTTTTAATT	GRCh37
NC_000016.8:g.46290034_46290035insTTAGAATTTTTTTATTTTTTTAATT	NCBI36
NG_016598.1:g.242324_242325insTTAGAATTTTTTTATTTTTTTAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1718+34_*1718+35insTTAGAATTTTTTTATTTTTTTAATT	ENSP00000512887.1:n.*1718+34_*1718+35insTTAGAATTTTTTTATTTTTTT...
ENST00000699276.1:c.*772+34_*772+35insTTAGAATTTTTTTATTTTTTTAATT	ENSP00000514257.1:n.*772+34_*772+35insTTAGAATTTTTTTATTTTTTTAA...
ENST00000323584.10:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT MANE Select	ENSP00000313504.5:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAA...
ENST00000299167.12:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	ENSP00000299167.8:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAA...
ENST00000323584.9:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	ENSP00000313504.5:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAA...
ENST00000564711.2:c.158+34_158+35insTTAGAATTTTTTTATTTTTTTAATT
ENST00000566044.5:c.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT	ENSP00000456729.1:n.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAA...
ENST00000566319.2:n.1960+34_1960+35insTTAGAATTTTTTTATTTTTTTAATT
NM_000293.2:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	NP_000284.1:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT
NM_001031835.2:c.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT	NP_001027005.1:n.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT
XM_005255983.3:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	XP_005256040.1:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT
XM_005255984.3:c.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT	XP_005256041.1:n.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT
XM_011523107.1:c.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT	XP_011521409.1:n.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT
NM_001363837.1:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	NP_001350766.1:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT
XM_005255983.4:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT	XP_005256040.1:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT
XM_005255984.4:c.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT	XP_005256041.1:n.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT
XM_017023282.1:c.2031+34_2031+35insTTAGAATTTTTTTATTTTTTTAATT	XP_016878771.1:n.2031+34_2031+35insTTAGAATTTTTTTATTTTTTTAATT
XM_017023283.1:c.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT	XP_016878772.1:n.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT
XM_017023284.1:c.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT	XP_016878773.1:n.1722+34_1722+35insTTAGAATTTTTTTATTTTTTTAATT
XR_001751913.1:n.3068+34_3068+35insTTAGAATTTTTTTATTTTTTTAATT
NM_000293.3:c.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT MANE Select	NP_000284.1:n.3144+34_3144+35insTTAGAATTTTTTTATTTTTTTAATT
NM_001031835.3:c.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT	NP_001027005.1:n.3123+34_3123+35insTTAGAATTTTTTTATTTTTTTAATT