Canonical Allele Identifier: CA409437309
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2146530917

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565436G>A , CM000682.2:g.57565436G>A GRCh38
NC_000020.10:g.56140492G>A , CM000682.1:g.56140492G>A GRCh37
NC_000020.9:g.55573898G>A NCBI36
NG_008205.1:g.9356G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1501G>A MANE Select ENSP00000319814.4:p.Ala501Thr
ENST00000319441.5:c.1501G>A ENSP00000319814.4:p.Ala501Thr
ENST00000467047.1:n.4143G>A
NM_002591.3:c.1501G>A NP_002582.3:p.Ala501Thr
XM_011528839.1:c.1105G>A XP_011527141.1:p.Ala369Thr
XM_024451888.1:c.1105G>A XP_024307656.1:p.Ala369Thr
NM_002591.4:c.1501G>A MANE Select NP_002582.3:p.Ala501Thr