Canonical Allele Identifier: CA2371897252
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57564751A= , CM000682.2:g.57564751A= GRCh38
NC_000020.10:g.56139807A= , CM000682.1:g.56139807A= GRCh37
NC_000020.9:g.55573213A= NCBI36
NG_008205.1:g.8671A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1318+138A= MANE Select ENSP00000319814.4:n.1318+138A=
ENST00000319441.5:c.1318+138A= ENSP00000319814.4:n.1318+138A=
ENST00000467047.1:n.3672A=
ENST00000485958.1:n.442+138A=
NM_002591.3:c.1318+138A= NP_002582.3:n.1318+138A=
XM_011528839.1:c.922+138A= XP_011527141.1:n.922+138A=
XM_024451888.1:c.922+138A= XP_024307656.1:n.922+138A=
NM_002591.4:c.1318+138A= MANE Select NP_002582.3:n.1318+138A=
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