Canonical Allele Identifier: CA511310993
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140503A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565447A>G , CM000682.2:g.57565447A>G GRCh38
NC_000020.10:g.56140503A>G , CM000682.1:g.56140503A>G GRCh37
NC_000020.9:g.55573909A>G NCBI36
NG_008205.1:g.9367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1512A>G MANE Select ENSP00000319814.4:p.Pro504=
ENST00000319441.5:c.1512A>G ENSP00000319814.4:p.Pro504=
ENST00000467047.1:n.4154A>G
NM_002591.3:c.1512A>G NP_002582.3:p.Pro504=
XM_011528839.1:c.1116A>G XP_011527141.1:p.Pro372=
XM_024451888.1:c.1116A>G XP_024307656.1:p.Pro372=
NM_002591.4:c.1512A>G MANE Select NP_002582.3:p.Pro504=