Canonical Allele Identifier: CA409435145
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2146527635

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562799G>C , CM000682.2:g.57562799G>C GRCh38
NC_000020.10:g.56137855G>C , CM000682.1:g.56137855G>C GRCh37
NC_000020.9:g.55571261G>C NCBI36
NG_008205.1:g.6719G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.510G>C MANE Select ENSP00000319814.4:p.Met170Ile
ENST00000319441.5:c.510G>C ENSP00000319814.4:p.Met170Ile
ENST00000467047.1:n.1720G>C
ENST00000498194.1:n.452G>C
NM_002591.3:c.510G>C NP_002582.3:p.Met170Ile
XM_011528839.1:c.114G>C XP_011527141.1:p.Met38Ile
XM_024451888.1:c.114G>C XP_024307656.1:p.Met38Ile
NM_002591.4:c.510G>C MANE Select NP_002582.3:p.Met170Ile