Canonical Allele Identifier: CA2371896384
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2070163362

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562975G>T , CM000682.2:g.57562975G>T GRCh38
NC_000020.10:g.56138031G>T , CM000682.1:g.56138031G>T GRCh37
NC_000020.9:g.55571437G>T NCBI36
NG_008205.1:g.6895G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-53G>T MANE Select ENSP00000319814.4:n.611-53G>T
ENST00000319441.5:c.611-53G>T ENSP00000319814.4:n.611-53G>T
ENST00000467047.1:n.1896G>T
ENST00000470051.1:n.142G>T
ENST00000498194.1:n.553-53G>T
NM_002591.3:c.611-53G>T NP_002582.3:n.611-53G>T
XM_011528839.1:c.215-53G>T XP_011527141.1:n.215-53G>T
XM_024451888.1:c.215-53G>T XP_024307656.1:n.215-53G>T
NM_002591.4:c.611-53G>T MANE Select NP_002582.3:n.611-53G>T