Canonical Allele Identifier: CA2371896406
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562996C= , CM000682.2:g.57562996C= GRCh38
NC_000020.10:g.56138052C= , CM000682.1:g.56138052C= GRCh37
NC_000020.9:g.55571458C= NCBI36
NG_008205.1:g.6916C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-32C= MANE Select ENSP00000319814.4:n.611-32C=
ENST00000319441.5:c.611-32C= ENSP00000319814.4:n.611-32C=
ENST00000467047.1:n.1917C=
ENST00000470051.1:n.163C=
ENST00000498194.1:n.553-32C=
NM_002591.3:c.611-32C= NP_002582.3:n.611-32C=
XM_011528839.1:c.215-32C= XP_011527141.1:n.215-32C=
XM_024451888.1:c.215-32C= XP_024307656.1:n.215-32C=
NM_002591.4:c.611-32C= MANE Select NP_002582.3:n.611-32C=