Canonical Allele Identifier: CA2371897642
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565593C= , CM000682.2:g.57565593C= GRCh38
NC_000020.10:g.56140649C= , CM000682.1:g.56140649C= GRCh37
NC_000020.9:g.55574055C= NCBI36
NG_008205.1:g.9513C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1658C= MANE Select ENSP00000319814.4:p.Thr553=
ENST00000319441.5:c.1658C= ENSP00000319814.4:p.Thr553=
ENST00000467047.1:n.4300C=
NM_002591.3:c.1658C= NP_002582.3:p.Thr553=
XM_011528839.1:c.1262C= XP_011527141.1:p.Thr421=
XM_024451888.1:c.1262C= XP_024307656.1:p.Thr421=
NM_002591.4:c.1658C= MANE Select NP_002582.3:p.Thr553=