Canonical Allele Identifier: CA2371897677
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565655A= , CM000682.2:g.57565655A= GRCh38
NC_000020.10:g.56140711A= , CM000682.1:g.56140711A= GRCh37
NC_000020.9:g.55574117A= NCBI36
NG_008205.1:g.9575A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1720A= MANE Select ENSP00000319814.4:p.Met574=
ENST00000319441.5:c.1720A= ENSP00000319814.4:p.Met574=
ENST00000467047.1:n.4362A=
NM_002591.3:c.1720A= NP_002582.3:p.Met574=
XM_011528839.1:c.1324A= XP_011527141.1:p.Met442=
XM_024451888.1:c.1324A= XP_024307656.1:p.Met442=
NM_002591.4:c.1720A= MANE Select NP_002582.3:p.Met574=