Canonical Allele Identifier: CA2371897557
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565412T= , CM000682.2:g.57565412T= GRCh38
NC_000020.10:g.56140468T= , CM000682.1:g.56140468T= GRCh37
NC_000020.9:g.55573874T= NCBI36
NG_008205.1:g.9332T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1477T= MANE Select ENSP00000319814.4:p.Tyr493=
ENST00000319441.5:c.1477T= ENSP00000319814.4:p.Tyr493=
ENST00000467047.1:n.4119T=
NM_002591.3:c.1477T= NP_002582.3:p.Tyr493=
XM_011528839.1:c.1081T= XP_011527141.1:p.Tyr361=
XM_024451888.1:c.1081T= XP_024307656.1:p.Tyr361=
NM_002591.4:c.1477T= MANE Select NP_002582.3:p.Tyr493=