Canonical Allele Identifier: CA2653461260
Gene: PCK1 HGNC NCBI

Linked Data

gnomAD v4: 20-57564823-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57564823T>G , CM000682.2:g.57564823T>G GRCh38
NC_000020.10:g.56139879T>G , CM000682.1:g.56139879T>G GRCh37
NC_000020.9:g.55573285T>G NCBI36
NG_008205.1:g.8743T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000319441.6:c.1318+210T>G MANE Select ENSP00000319814.4:n.1318+210T>G
ENST00000319441.5:c.1318+210T>G ENSP00000319814.4:n.1318+210T>G
ENST00000467047.1:n.3744T>G
ENST00000485958.1:n.442+210T>G
NM_002591.3:c.1318+210T>G NP_002582.3:n.1318+210T>G
XM_011528839.1:c.922+210T>G XP_011527141.1:n.922+210T>G
XM_024451888.1:c.922+210T>G XP_024307656.1:n.922+210T>G
NM_002591.4:c.1318+210T>G MANE Select NP_002582.3:n.1318+210T>G
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