Canonical Allele Identifier: CA2816822634
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562988_57562989insTA , CM000682.2:g.57562988_57562989insTA GRCh38
NC_000020.10:g.56138044_56138045insTA , CM000682.1:g.56138044_56138045insTA GRCh37
NC_000020.9:g.55571450_55571451insTA NCBI36
NG_008205.1:g.6908_6909insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-40_611-39insTA MANE Select ENSP00000319814.4:n.611-40_611-39insTA
ENST00000319441.5:c.611-40_611-39insTA ENSP00000319814.4:n.611-40_611-39insTA
ENST00000467047.1:n.1909_1910insTA
ENST00000470051.1:n.155_156insTA
ENST00000498194.1:n.553-40_553-39insTA
NM_002591.3:c.611-40_611-39insTA NP_002582.3:n.611-40_611-39insTA
XM_011528839.1:c.215-40_215-39insTA XP_011527141.1:n.215-40_215-39insTA
XM_024451888.1:c.215-40_215-39insTA XP_024307656.1:n.215-40_215-39insTA
NM_002591.4:c.611-40_611-39insTA MANE Select NP_002582.3:n.611-40_611-39insTA