Canonical Allele Identifier: CA2371896395
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562986_57562987delinsAG , CM000682.2:g.57562986_57562987delinsAG GRCh38
NC_000020.10:g.56138042_56138043delinsAG , CM000682.1:g.56138042_56138043delinsAG GRCh37
NC_000020.9:g.55571448_55571449delinsAG NCBI36
NG_008205.1:g.6906_6907delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-42_611-41delinsAG MANE Select ENSP00000319814.4:n.611-42_611-41delinsAG
ENST00000319441.5:c.611-42_611-41delinsAG ENSP00000319814.4:n.611-42_611-41delinsAG
ENST00000467047.1:n.1907_1908delinsAG
ENST00000470051.1:n.153_154delinsAG
ENST00000498194.1:n.553-42_553-41delinsAG
NM_002591.3:c.611-42_611-41delinsAG NP_002582.3:n.611-42_611-41delinsAG
XM_011528839.1:c.215-42_215-41delinsAG XP_011527141.1:n.215-42_215-41delinsAG
XM_024451888.1:c.215-42_215-41delinsAG XP_024307656.1:n.215-42_215-41delinsAG
NM_002591.4:c.611-42_611-41delinsAG MANE Select NP_002582.3:n.611-42_611-41delinsAG