Canonical Allele Identifier: CA2371896375
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562962T= , CM000682.2:g.57562962T= GRCh38
NC_000020.10:g.56138018T= , CM000682.1:g.56138018T= GRCh37
NC_000020.9:g.55571424T= NCBI36
NG_008205.1:g.6882T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.610+63T= MANE Select ENSP00000319814.4:n.610+63T=
ENST00000319441.5:c.610+63T= ENSP00000319814.4:n.610+63T=
ENST00000467047.1:n.1883T=
ENST00000470051.1:n.129T=
ENST00000498194.1:n.552+63T=
NM_002591.3:c.610+63T= NP_002582.3:n.610+63T=
XM_011528839.1:c.214+63T= XP_011527141.1:n.214+63T=
XM_024451888.1:c.214+63T= XP_024307656.1:n.214+63T=
NM_002591.4:c.610+63T= MANE Select NP_002582.3:n.610+63T=