Canonical Allele Identifier: CA2371897538
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565356T= , CM000682.2:g.57565356T= GRCh38
NC_000020.10:g.56140412T= , CM000682.1:g.56140412T= GRCh37
NC_000020.9:g.55573818T= NCBI36
NG_008205.1:g.9276T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1421T= MANE Select ENSP00000319814.4:p.Ile474=
ENST00000319441.5:c.1421T= ENSP00000319814.4:p.Ile474=
ENST00000467047.1:n.4063T=
ENST00000485958.1:n.545T=
NM_002591.3:c.1421T= NP_002582.3:p.Ile474=
XM_011528839.1:c.1025T= XP_011527141.1:p.Ile342=
XM_024451888.1:c.1025T= XP_024307656.1:p.Ile342=
NM_002591.4:c.1421T= MANE Select NP_002582.3:p.Ile474=