Canonical Allele Identifier: CA409435076
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56137822G>C (hg19) chr20:g.57562766G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562766G>C , CM000682.2:g.57562766G>C GRCh38
NC_000020.10:g.56137822G>C , CM000682.1:g.56137822G>C GRCh37
NC_000020.9:g.55571228G>C NCBI36
NG_008205.1:g.6686G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.477G>C MANE Select ENSP00000319814.4:p.Glu159Asp
ENST00000319441.5:c.477G>C ENSP00000319814.4:p.Glu159Asp
ENST00000467047.1:n.1687G>C
ENST00000498194.1:n.419G>C
NM_002591.3:c.477G>C NP_002582.3:p.Glu159Asp
XM_011528839.1:c.81G>C XP_011527141.1:p.Glu27Asp
XM_024451888.1:c.81G>C XP_024307656.1:p.Glu27Asp
NM_002591.4:c.477G>C MANE Select NP_002582.3:p.Glu159Asp
Search 100 bp 5'
Search 100 bp 3'