Canonical Allele Identifier: CA2371897590
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565479A= , CM000682.2:g.57565479A= GRCh38
NC_000020.10:g.56140535A= , CM000682.1:g.56140535A= GRCh37
NC_000020.9:g.55573941A= NCBI36
NG_008205.1:g.9399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1544A= MANE Select ENSP00000319814.4:p.Asn515=
ENST00000319441.5:c.1544A= ENSP00000319814.4:p.Asn515=
ENST00000467047.1:n.4186A=
NM_002591.3:c.1544A= NP_002582.3:p.Asn515=
XM_011528839.1:c.1148A= XP_011527141.1:p.Asn383=
XM_024451888.1:c.1148A= XP_024307656.1:p.Asn383=
NM_002591.4:c.1544A= MANE Select NP_002582.3:p.Asn515=