Canonical Allele Identifier: CA2653461279
Gene: PCK1 HGNC NCBI

Linked Data

gnomAD v4: 20-57564830-T-TCTG
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57564830_57564831insCTG , CM000682.2:g.57564830_57564831insCTG GRCh38
NC_000020.10:g.56139886_56139887insCTG , CM000682.1:g.56139886_56139887insCTG GRCh37
NC_000020.9:g.55573292_55573293insCTG NCBI36
NG_008205.1:g.8750_8751insCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000319441.6:c.1319-210_1319-209insCTG MANE Select ENSP00000319814.4:n.1319-210_1319-209insC...
ENST00000319441.5:c.1319-210_1319-209insCTG ENSP00000319814.4:n.1319-210_1319-209insC...
ENST00000467047.1:n.3751_3752insCTG
ENST00000485958.1:n.443-210_443-209insCTG
NM_002591.3:c.1319-210_1319-209insCTG NP_002582.3:n.1319-210_1319-209insCTG
XM_011528839.1:c.923-210_923-209insCTG XP_011527141.1:n.923-210_923-209insCTG
XM_024451888.1:c.923-210_923-209insCTG XP_024307656.1:n.923-210_923-209insCTG
NM_002591.4:c.1319-210_1319-209insCTG MANE Select NP_002582.3:n.1319-210_1319-209insCTG
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