Canonical Allele Identifier: CA409437612
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140627G>T (hg19) chr20:g.57565571G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565571G>T , CM000682.2:g.57565571G>T GRCh38
NC_000020.10:g.56140627G>T , CM000682.1:g.56140627G>T GRCh37
NC_000020.9:g.55574033G>T NCBI36
NG_008205.1:g.9491G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1636G>T MANE Select ENSP00000319814.4:p.Gly546Ter
ENST00000319441.5:c.1636G>T ENSP00000319814.4:p.Gly546Ter
ENST00000467047.1:n.4278G>T
NM_002591.3:c.1636G>T NP_002582.3:p.Gly546Ter
XM_011528839.1:c.1240G>T XP_011527141.1:p.Gly414Ter
XM_024451888.1:c.1240G>T XP_024307656.1:p.Gly414Ter
NM_002591.4:c.1636G>T MANE Select NP_002582.3:p.Gly546Ter
Search 100 bp 5'
Search 100 bp 3'