Canonical Allele Identifier: CA721060291

Gene: PHKB

Linked Data

• dbSNP Id: rs759138119
• MyVariant Identifiers: chr16:g.47732707_47732709del (hg19) ; chr16:g.47698796_47698798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47698799_47698801del , CM000678.2:g.47698799_47698801del	GRCh38
NC_000016.9:g.47732710_47732712del , CM000678.1:g.47732710_47732712del	GRCh37
NC_000016.8:g.46290211_46290213del	NCBI36
NG_016598.1:g.242501_242503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1718+211_*1718+213del	ENSP00000512887.1:n.*1718+211_*1718+213del
ENST00000699276.1:c.*772+211_*772+213del	ENSP00000514257.1:n.*772+211_*772+213del
ENST00000323584.10:c.3144+211_3144+213del MANE Select	ENSP00000313504.5:n.3144+211_3144+213del
ENST00000299167.12:c.3144+211_3144+213del	ENSP00000299167.8:n.3144+211_3144+213del
ENST00000323584.9:c.3144+211_3144+213del	ENSP00000313504.5:n.3144+211_3144+213del
ENST00000564711.2:c.158+211_158+213del
ENST00000566044.5:c.3123+211_3123+213del	ENSP00000456729.1:n.3123+211_3123+213del
ENST00000566319.2:n.1960+211_1960+213del
NM_000293.2:c.3144+211_3144+213del	NP_000284.1:n.3144+211_3144+213del
NM_001031835.2:c.3123+211_3123+213del	NP_001027005.1:n.3123+211_3123+213del
XM_005255983.3:c.3144+211_3144+213del	XP_005256040.1:n.3144+211_3144+213del
XM_005255984.3:c.3123+211_3123+213del	XP_005256041.1:n.3123+211_3123+213del
XM_011523107.1:c.1722+211_1722+213del	XP_011521409.1:n.1722+211_1722+213del
NM_001363837.1:c.3144+211_3144+213del	NP_001350766.1:n.3144+211_3144+213del
XM_005255983.4:c.3144+211_3144+213del	XP_005256040.1:n.3144+211_3144+213del
XM_005255984.4:c.3123+211_3123+213del	XP_005256041.1:n.3123+211_3123+213del
XM_017023282.1:c.2031+211_2031+213del	XP_016878771.1:n.2031+211_2031+213del
XM_017023283.1:c.1722+211_1722+213del	XP_016878772.1:n.1722+211_1722+213del
XM_017023284.1:c.1722+211_1722+213del	XP_016878773.1:n.1722+211_1722+213del
XR_001751913.1:n.3068+211_3068+213del
NM_000293.3:c.3144+211_3144+213del MANE Select	NP_000284.1:n.3144+211_3144+213del
NM_001031835.3:c.3123+211_3123+213del	NP_001027005.1:n.3123+211_3123+213del