Canonical Allele Identifier: CA316278829
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs771118313

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562728G>C , CM000682.2:g.57562728G>C GRCh38
NC_000020.10:g.56137784G>C , CM000682.1:g.56137784G>C GRCh37
NC_000020.9:g.55571190G>C NCBI36
NG_008205.1:g.6648G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.439G>C MANE Select ENSP00000319814.4:p.Gly147Arg
ENST00000319441.5:c.439G>C ENSP00000319814.4:p.Gly147Arg
ENST00000467047.1:n.1649G>C
ENST00000498194.1:n.381G>C
NM_002591.3:c.439G>C NP_002582.3:p.Gly147Arg
XM_011528839.1:c.43G>C XP_011527141.1:p.Gly15Arg
XM_024451888.1:c.43G>C XP_024307656.1:p.Gly15Arg
NM_002591.4:c.439G>C MANE Select NP_002582.3:p.Gly147Arg