Canonical Allele Identifier: CA409436500
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56139407A>G (hg19) chr20:g.57564351A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57564351A>G , CM000682.2:g.57564351A>G GRCh38
NC_000020.10:g.56139407A>G , CM000682.1:g.56139407A>G GRCh37
NC_000020.9:g.55572813A>G NCBI36
NG_008205.1:g.8271A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000319441.6:c.1144A>G MANE Select ENSP00000319814.4:p.Thr382Ala
ENST00000319441.5:c.1144A>G ENSP00000319814.4:p.Thr382Ala
ENST00000467047.1:n.3272A>G
ENST00000485958.1:n.268A>G
NM_002591.3:c.1144A>G NP_002582.3:p.Thr382Ala
XM_011528839.1:c.748A>G XP_011527141.1:p.Thr250Ala
XM_024451888.1:c.748A>G XP_024307656.1:p.Thr250Ala
NM_002591.4:c.1144A>G MANE Select NP_002582.3:p.Thr382Ala
Search 100 bp 5'
Search 100 bp 3'