Canonical Allele Identifier: CA2816822537
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562665C>T , CM000682.2:g.57562665C>T GRCh38
NC_000020.10:g.56137721C>T , CM000682.1:g.56137721C>T GRCh37
NC_000020.9:g.55571127C>T NCBI36
NG_008205.1:g.6585C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-31C>T MANE Select ENSP00000319814.4:n.407-31C>T
ENST00000319441.5:c.407-31C>T ENSP00000319814.4:n.407-31C>T
ENST00000467047.1:n.1586C>T
ENST00000498194.1:n.318C>T
NM_002591.3:c.407-31C>T NP_002582.3:n.407-31C>T
XM_011528839.1:c.11-31C>T XP_011527141.1:n.11-31C>T
XM_024451888.1:c.11-31C>T XP_024307656.1:n.11-31C>T
NM_002591.4:c.407-31C>T MANE Select NP_002582.3:n.407-31C>T