Canonical Allele Identifier: CA636606516
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs1341759721

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562982A>G , CM000682.2:g.57562982A>G GRCh38
NC_000020.10:g.56138038A>G , CM000682.1:g.56138038A>G GRCh37
NC_000020.9:g.55571444A>G NCBI36
NG_008205.1:g.6902A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-46A>G MANE Select ENSP00000319814.4:n.611-46A>G
ENST00000319441.5:c.611-46A>G ENSP00000319814.4:n.611-46A>G
ENST00000467047.1:n.1903A>G
ENST00000470051.1:n.149A>G
ENST00000498194.1:n.553-46A>G
NM_002591.3:c.611-46A>G NP_002582.3:n.611-46A>G
XM_011528839.1:c.215-46A>G XP_011527141.1:n.215-46A>G
XM_024451888.1:c.215-46A>G XP_024307656.1:n.215-46A>G
NM_002591.4:c.611-46A>G MANE Select NP_002582.3:n.611-46A>G