Canonical Allele Identifier: CA511310965
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140443C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565387C>G , CM000682.2:g.57565387C>G GRCh38
NC_000020.10:g.56140443C>G , CM000682.1:g.56140443C>G GRCh37
NC_000020.9:g.55573849C>G NCBI36
NG_008205.1:g.9307C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1452C>G MANE Select ENSP00000319814.4:p.Pro484=
ENST00000319441.5:c.1452C>G ENSP00000319814.4:p.Pro484=
ENST00000467047.1:n.4094C>G
ENST00000485958.1:n.576C>G
NM_002591.3:c.1452C>G NP_002582.3:p.Pro484=
XM_011528839.1:c.1056C>G XP_011527141.1:p.Pro352=
XM_024451888.1:c.1056C>G XP_024307656.1:p.Pro352=
NM_002591.4:c.1452C>G MANE Select NP_002582.3:p.Pro484=
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