Canonical Allele Identifier: CA2806482175

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753446_30753447insATA , CM000678.2:g.30753446_30753447insATA	GRCh38
NC_000016.9:g.30764767_30764768insATA , CM000678.1:g.30764767_30764768insATA	GRCh37
NC_000016.8:g.30672268_30672269insATA	NCBI36
NG_016616.1:g.10148_10149insATA
NG_016616.2:g.10148_10149insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.445_446insATA MANE Select	ENSP00000455607.1:p.Asn148_Ile149insAsn
ENST00000328273.11:c.445_446insATA	ENSP00000329968.7:p.Asn148_Ile149insAsn
ENST00000424889.7:c.445_446insATA	ENSP00000388571.3:p.Asn148_Ile149insAsn
ENST00000561712.1:c.119_120insATA
ENST00000563588.5:c.445_446insATA	ENSP00000455607.1:p.Asn148_Ile149insAsn
ENST00000563607.1:c.*117_*118insATA	ENSP00000454641.1:n.*117_*118insATA
ENST00000563913.5:n.778_779insATA
ENST00000564838.5:n.819_820insATA
ENST00000565897.5:c.445_446insATA	ENSP00000457359.1:p.Asn148_Ile149insAsn
ENST00000565924.5:c.445_446insATA	ENSP00000455091.1:p.Asn148_Ile149insAsn
ENST00000569684.1:n.857_858insATA
NM_000294.2:c.445_446insATA	NP_000285.1:p.Asn148_Ile149insAsn
NM_001172432.1:c.445_446insATA	NP_001165903.1:p.Asn148_Ile149insAsn
NM_000294.3:c.445_446insATA MANE Select	NP_000285.1:p.Asn148_Ile149insAsn
NM_001172432.2:c.445_446insATA	NP_001165903.1:p.Asn148_Ile149insAsn