Canonical Allele Identifier: CA2371896276
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562805C= , CM000682.2:g.57562805C= GRCh38
NC_000020.10:g.56137861C= , CM000682.1:g.56137861C= GRCh37
NC_000020.9:g.55571267C= NCBI36
NG_008205.1:g.6725C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.516C= MANE Select ENSP00000319814.4:p.Ile172=
ENST00000319441.5:c.516C= ENSP00000319814.4:p.Ile172=
ENST00000467047.1:n.1726C=
ENST00000498194.1:n.458C=
NM_002591.3:c.516C= NP_002582.3:p.Ile172=
XM_011528839.1:c.120C= XP_011527141.1:p.Ile40=
XM_024451888.1:c.120C= XP_024307656.1:p.Ile40=
NM_002591.4:c.516C= MANE Select NP_002582.3:p.Ile172=