Canonical Allele Identifier: CA2371897635
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565573A= , CM000682.2:g.57565573A= GRCh38
NC_000020.10:g.56140629A= , CM000682.1:g.56140629A= GRCh37
NC_000020.9:g.55574035A= NCBI36
NG_008205.1:g.9493A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1638A= MANE Select ENSP00000319814.4:p.Gly546=
ENST00000319441.5:c.1638A= ENSP00000319814.4:p.Gly546=
ENST00000467047.1:n.4280A=
NM_002591.3:c.1638A= NP_002582.3:p.Gly546=
XM_011528839.1:c.1242A= XP_011527141.1:p.Gly414=
XM_024451888.1:c.1242A= XP_024307656.1:p.Gly414=
NM_002591.4:c.1638A= MANE Select NP_002582.3:p.Gly546=
Search 100 bp 5'
Search 100 bp 3'