Canonical Allele Identifier: CA2371896396
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562986_57562997delinsAGGGCCCTGGCG , CM000682.2:g.57562986_57562997delinsAGGGCCCTGGCG GRCh38
NC_000020.10:g.56138042_56138053delinsAGGGCCCTGGCG , CM000682.1:g.56138042_56138053delinsAGGGCCCTGGCG GRCh37
NC_000020.9:g.55571448_55571459delinsAGGGCCCTGGCG NCBI36
NG_008205.1:g.6906_6917delinsAGGGCCCTGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-42_611-31delinsAGGGCCCTGGCG MANE Select ENSP00000319814.4:n.611-42_611-31delinsAGGGCCCTGGCG
ENST00000319441.5:c.611-42_611-31delinsAGGGCCCTGGCG ENSP00000319814.4:n.611-42_611-31delinsAGGGCCCTGGCG
ENST00000467047.1:n.1907_1918delinsAGGGCCCTGGCG
ENST00000470051.1:n.153_164delinsAGGGCCCTGGCG
ENST00000498194.1:n.553-42_553-31delinsAGGGCCCTGGCG
NM_002591.3:c.611-42_611-31delinsAGGGCCCTGGCG NP_002582.3:n.611-42_611-31delinsAGGGCCCTGGCG
XM_011528839.1:c.215-42_215-31delinsAGGGCCCTGGCG XP_011527141.1:n.215-42_215-31delinsAGGGCCCTGGCG
XM_024451888.1:c.215-42_215-31delinsAGGGCCCTGGCG XP_024307656.1:n.215-42_215-31delinsAGGGCCCTGGCG
NM_002591.4:c.611-42_611-31delinsAGGGCCCTGGCG MANE Select NP_002582.3:n.611-42_611-31delinsAGGGCCCTGGCG