Canonical Allele Identifier: CA2371896385
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562976_57562977delinsAC , CM000682.2:g.57562976_57562977delinsAC GRCh38
NC_000020.10:g.56138032_56138033delinsAC , CM000682.1:g.56138032_56138033delinsAC GRCh37
NC_000020.9:g.55571438_55571439delinsAC NCBI36
NG_008205.1:g.6896_6897delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-52_611-51delinsAC MANE Select ENSP00000319814.4:n.611-52_611-51delinsAC
ENST00000319441.5:c.611-52_611-51delinsAC ENSP00000319814.4:n.611-52_611-51delinsAC
ENST00000467047.1:n.1897_1898delinsAC
ENST00000470051.1:n.143_144delinsAC
ENST00000498194.1:n.553-52_553-51delinsAC
NM_002591.3:c.611-52_611-51delinsAC NP_002582.3:n.611-52_611-51delinsAC
XM_011528839.1:c.215-52_215-51delinsAC XP_011527141.1:n.215-52_215-51delinsAC
XM_024451888.1:c.215-52_215-51delinsAC XP_024307656.1:n.215-52_215-51delinsAC
NM_002591.4:c.611-52_611-51delinsAC MANE Select NP_002582.3:n.611-52_611-51delinsAC