Canonical Allele Identifier: CA2371896387
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562979C= , CM000682.2:g.57562979C= GRCh38
NC_000020.10:g.56138035C= , CM000682.1:g.56138035C= GRCh37
NC_000020.9:g.55571441C= NCBI36
NG_008205.1:g.6899C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-49C= MANE Select ENSP00000319814.4:n.611-49C=
ENST00000319441.5:c.611-49C= ENSP00000319814.4:n.611-49C=
ENST00000467047.1:n.1900C=
ENST00000470051.1:n.146C=
ENST00000498194.1:n.553-49C=
NM_002591.3:c.611-49C= NP_002582.3:n.611-49C=
XM_011528839.1:c.215-49C= XP_011527141.1:n.215-49C=
XM_024451888.1:c.215-49C= XP_024307656.1:n.215-49C=
NM_002591.4:c.611-49C= MANE Select NP_002582.3:n.611-49C=
Search 100 bp 5'
Search 100 bp 3'