Canonical Allele Identifier: CA396097174

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47497402C>G , CM000678.2:g.47497402C>G	GRCh38
NC_000016.9:g.47531313C>G , CM000678.1:g.47531313C>G	GRCh37
NC_000016.8:g.46088814C>G	NCBI36
NG_016598.1:g.41104C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000293.3:c.80C>G MANE Select	NP_000284.1:p.Ser27Ter
ENST00000323584.10:c.80C>G MANE Select	ENSP00000313504.5:p.Ser27Ter
NM_000293.2:c.80C>G	NP_000284.1:p.Ser27Ter
NM_001031835.2:c.59C>G	NP_001027005.1:p.Ser20Ter
NM_001031835.3:c.59C>G	NP_001027005.1:p.Ser20Ter
NM_001363837.1:c.80C>G	NP_001350766.1:p.Ser27Ter
ENST00000299167.12:c.80C>G	ENSP00000299167.8:p.Ser27Ter
ENST00000323584.9:c.80C>G	ENSP00000313504.5:p.Ser27Ter
ENST00000563376.5:c.59C>G	ENSP00000457905.1:p.Ser20Ter
ENST00000564873.1:c.59C>G	ENSP00000460408.1:p.Ser20Ter
ENST00000565424.2:n.96+35976C>G
ENST00000566037.6:c.59C>G	ENSP00000455664.2:p.Ser20Ter
ENST00000566044.5:c.59C>G	ENSP00000456729.1:p.Ser20Ter
ENST00000567402.5:n.95C>G
ENST00000696809.1:c.59C>G	ENSP00000512887.1:p.Ser20Ter
ENST00000699276.1:c.59C>G	ENSP00000514257.1:p.Ser20Ter
XM_005255983.3:c.80C>G	XP_005256040.1:p.Ser27Ter
XM_005255983.4:c.80C>G	XP_005256040.1:p.Ser27Ter
XM_005255984.3:c.59C>G	XP_005256041.1:p.Ser20Ter
XM_005255984.4:c.59C>G	XP_005256041.1:p.Ser20Ter
XM_011523106.1:c.80C>G	XP_011521408.1:p.Ser27Ter
XM_017023283.1:c.-1426C>G	XP_016878772.1:n.-1426C>G
XM_017023284.1:c.-1426C>G	XP_016878773.1:n.-1426C>G
XR_001751913.1:n.95C>G