Canonical Allele Identifier: CA2371897629
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565565A= , CM000682.2:g.57565565A= GRCh38
NC_000020.10:g.56140621A= , CM000682.1:g.56140621A= GRCh37
NC_000020.9:g.55574027A= NCBI36
NG_008205.1:g.9485A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1630A= MANE Select ENSP00000319814.4:p.Ile544=
ENST00000319441.5:c.1630A= ENSP00000319814.4:p.Ile544=
ENST00000467047.1:n.4272A=
NM_002591.3:c.1630A= NP_002582.3:p.Ile544=
XM_011528839.1:c.1234A= XP_011527141.1:p.Ile412=
XM_024451888.1:c.1234A= XP_024307656.1:p.Ile412=
NM_002591.4:c.1630A= MANE Select NP_002582.3:p.Ile544=
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