Canonical Allele Identifier: CA511310950
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140413C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565357C>T , CM000682.2:g.57565357C>T GRCh38
NC_000020.10:g.56140413C>T , CM000682.1:g.56140413C>T GRCh37
NC_000020.9:g.55573819C>T NCBI36
NG_008205.1:g.9277C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1422C>T MANE Select ENSP00000319814.4:p.Ile474=
ENST00000319441.5:c.1422C>T ENSP00000319814.4:p.Ile474=
ENST00000467047.1:n.4064C>T
ENST00000485958.1:n.546C>T
NM_002591.3:c.1422C>T NP_002582.3:p.Ile474=
XM_011528839.1:c.1026C>T XP_011527141.1:p.Ile342=
XM_024451888.1:c.1026C>T XP_024307656.1:p.Ile342=
NM_002591.4:c.1422C>T MANE Select NP_002582.3:p.Ile474=