Canonical Allele Identifier: CA395656749

Gene: PHKG2

Linked Data

• MyVariant Identifiers: chr16:g.30764807A>T (hg19) ; chr16:g.30753486A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753486A>T , CM000678.2:g.30753486A>T	GRCh38
NC_000016.9:g.30764807A>T , CM000678.1:g.30764807A>T	GRCh37
NC_000016.8:g.30672308A>T	NCBI36
NG_016616.1:g.10188A>T
NG_016616.2:g.10188A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.485A>T MANE Select	ENSP00000455607.1:p.Asp162Val
ENST00000328273.11:c.485A>T	ENSP00000329968.7:p.Asp162Val
ENST00000424889.7:c.485A>T	ENSP00000388571.3:p.Asp162Val
ENST00000561712.1:c.159A>T
ENST00000563588.5:c.485A>T	ENSP00000455607.1:p.Asp162Val
ENST00000563607.1:c.*157A>T	ENSP00000454641.1:n.*157A>T
ENST00000563913.5:n.818A>T
ENST00000564838.5:n.859A>T
ENST00000565897.5:c.485A>T	ENSP00000457359.1:p.Asp162Val
ENST00000565924.5:c.485A>T	ENSP00000455091.1:p.Asp162Val
ENST00000569684.1:n.897A>T
NM_000294.2:c.485A>T	NP_000285.1:p.Asp162Val
NM_001172432.1:c.485A>T	NP_001165903.1:p.Asp162Val
NM_000294.3:c.485A>T MANE Select	NP_000285.1:p.Asp162Val
NM_001172432.2:c.485A>T	NP_001165903.1:p.Asp162Val