Canonical Allele Identifier: CA2371897571
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565441G= , CM000682.2:g.57565441G= GRCh38
NC_000020.10:g.56140497G= , CM000682.1:g.56140497G= GRCh37
NC_000020.9:g.55573903G= NCBI36
NG_008205.1:g.9361G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1506G= MANE Select ENSP00000319814.4:p.Gln502=
ENST00000319441.5:c.1506G= ENSP00000319814.4:p.Gln502=
ENST00000467047.1:n.4148G=
NM_002591.3:c.1506G= NP_002582.3:p.Gln502=
XM_011528839.1:c.1110G= XP_011527141.1:p.Gln370=
XM_024451888.1:c.1110G= XP_024307656.1:p.Gln370=
NM_002591.4:c.1506G= MANE Select NP_002582.3:p.Gln502=