Canonical Allele Identifier: CA511311064
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140635C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565579C>T , CM000682.2:g.57565579C>T GRCh38
NC_000020.10:g.56140635C>T , CM000682.1:g.56140635C>T GRCh37
NC_000020.9:g.55574041C>T NCBI36
NG_008205.1:g.9499C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1644C>T MANE Select ENSP00000319814.4:p.Ala548=
ENST00000319441.5:c.1644C>T ENSP00000319814.4:p.Ala548=
ENST00000467047.1:n.4286C>T
NM_002591.3:c.1644C>T NP_002582.3:p.Ala548=
XM_011528839.1:c.1248C>T XP_011527141.1:p.Ala416=
XM_024451888.1:c.1248C>T XP_024307656.1:p.Ala416=
NM_002591.4:c.1644C>T MANE Select NP_002582.3:p.Ala548=
Search 100 bp 5'
Search 100 bp 3'