Canonical Allele Identifier: CA409437171
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140432G>A (hg19) chr20:g.57565376G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565376G>A , CM000682.2:g.57565376G>A GRCh38
NC_000020.10:g.56140432G>A , CM000682.1:g.56140432G>A GRCh37
NC_000020.9:g.55573838G>A NCBI36
NG_008205.1:g.9296G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1441G>A MANE Select ENSP00000319814.4:p.Ala481Thr
ENST00000319441.5:c.1441G>A ENSP00000319814.4:p.Ala481Thr
ENST00000467047.1:n.4083G>A
ENST00000485958.1:n.565G>A
NM_002591.3:c.1441G>A NP_002582.3:p.Ala481Thr
XM_011528839.1:c.1045G>A XP_011527141.1:p.Ala349Thr
XM_024451888.1:c.1045G>A XP_024307656.1:p.Ala349Thr
NM_002591.4:c.1441G>A MANE Select NP_002582.3:p.Ala481Thr
Search 100 bp 5'
Search 100 bp 3'