Canonical Allele Identifier: CA2371897542
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565369C= , CM000682.2:g.57565369C= GRCh38
NC_000020.10:g.56140425C= , CM000682.1:g.56140425C= GRCh37
NC_000020.9:g.55573831C= NCBI36
NG_008205.1:g.9289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1434C= MANE Select ENSP00000319814.4:p.Asp478=
ENST00000319441.5:c.1434C= ENSP00000319814.4:p.Asp478=
ENST00000467047.1:n.4076C=
ENST00000485958.1:n.558C=
NM_002591.3:c.1434C= NP_002582.3:p.Asp478=
XM_011528839.1:c.1038C= XP_011527141.1:p.Asp346=
XM_024451888.1:c.1038C= XP_024307656.1:p.Asp346=
NM_002591.4:c.1434C= MANE Select NP_002582.3:p.Asp478=