Canonical Allele Identifier: CA2371897665
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565631C= , CM000682.2:g.57565631C= GRCh38
NC_000020.10:g.56140687C= , CM000682.1:g.56140687C= GRCh37
NC_000020.9:g.55574093C= NCBI36
NG_008205.1:g.9551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1696C= MANE Select ENSP00000319814.4:p.Leu566=
ENST00000319441.5:c.1696C= ENSP00000319814.4:p.Leu566=
ENST00000467047.1:n.4338C=
NM_002591.3:c.1696C= NP_002582.3:p.Leu566=
XM_011528839.1:c.1300C= XP_011527141.1:p.Leu434=
XM_024451888.1:c.1300C= XP_024307656.1:p.Leu434=
NM_002591.4:c.1696C= MANE Select NP_002582.3:p.Leu566=