Canonical Allele Identifier: CA511310863
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56137825G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562769G>A , CM000682.2:g.57562769G>A GRCh38
NC_000020.10:g.56137825G>A , CM000682.1:g.56137825G>A GRCh37
NC_000020.9:g.55571231G>A NCBI36
NG_008205.1:g.6689G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.480G>A MANE Select ENSP00000319814.4:p.Leu160=
ENST00000319441.5:c.480G>A ENSP00000319814.4:p.Leu160=
ENST00000467047.1:n.1690G>A
ENST00000498194.1:n.422G>A
NM_002591.3:c.480G>A NP_002582.3:p.Leu160=
XM_011528839.1:c.84G>A XP_011527141.1:p.Leu28=
XM_024451888.1:c.84G>A XP_024307656.1:p.Leu28=
NM_002591.4:c.480G>A MANE Select NP_002582.3:p.Leu160=
Search 100 bp 5'
Search 100 bp 3'